ClinVar for Gene (Select 89790) - ClinVar

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Links from Gene

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3162142	NM_033130.5(SIGLEC10):c.914C>T (p.Pro305Leu)	SIGLEC10, SIGLEC10-AS1 (P247L +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3162141	NM_033130.5(SIGLEC10):c.797C>T (p.Ala266Val)	SIGLEC10, SIGLEC10-AS1 (A208V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3162140	NM_033130.5(SIGLEC10):c.65G>T (p.Trp22Leu)	SIGLEC10, SIGLEC10-AS1 (W22L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3162139	NM_033130.5(SIGLEC10):c.575C>A (p.Pro192Gln)	SIGLEC10, SIGLEC10-AS1 (P144Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3162138	NM_033130.5(SIGLEC10):c.547G>A (p.Ala183Thr)	SIGLEC10, SIGLEC10-AS1 (A183T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3162137	NM_033130.5(SIGLEC10):c.2066C>T (p.Ala689Val)	SIGLEC10 (A504V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162136	NM_033130.5(SIGLEC10):c.1958C>T (p.Thr653Ile)	SIGLEC10 (T510I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162135	NM_033130.5(SIGLEC10):c.1855A>G (p.Ser619Gly)	SIGLEC10 (S466G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162133	NM_033130.5(SIGLEC10):c.1735A>G (p.Thr579Ala)	SIGLEC10 (T426A +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3162132	NM_033130.5(SIGLEC10):c.1710C>T (p.Ile570=)	SIGLEC10	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3162131	NM_033130.5(SIGLEC10):c.1125C>G (p.Ser375Arg)	SIGLEC10 (S285R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2650376	NM_033130.5(SIGLEC10):c.939G>A (p.Val313=)	SIGLEC10-AS1, SIGLEC10	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2650375	NM_033130.5(SIGLEC10):c.941A>G (p.Lys314Arg)	SIGLEC10, SIGLEC10-AS1 (K256R +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2650374	NM_033130.5(SIGLEC10):c.945T>C (p.Ala315=)	SIGLEC10, SIGLEC10-AS1	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2590381	NM_033130.5(SIGLEC10):c.688G>T (p.Val230Phe)	SIGLEC10, SIGLEC10-AS1 (D90E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590380	NM_033130.5(SIGLEC10):c.1786G>C (p.Asp596His)	SIGLEC10 (D453H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568775	NM_033130.5(SIGLEC10):c.259C>T (p.Arg87Trp)	SIGLEC10, SIGLEC10-AS1 (R87W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2558158	NM_033130.5(SIGLEC10):c.1651G>A (p.Gly551Arg)	SIGLEC10 (G366R +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554685	NM_033130.5(SIGLEC10):c.449T>C (p.Ile150Thr)	SIGLEC10, SIGLEC10-AS1 (I150T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554013	NM_033130.5(SIGLEC10):c.244G>C (p.Val82Leu)	SIGLEC10, SIGLEC10-AS1 (V82L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2520767	NM_033130.5(SIGLEC10):c.920G>A (p.Gly307Glu)	SIGLEC10, SIGLEC10-AS1 (G249E +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 2493240	NM_033130.5(SIGLEC10):c.1051G>A (p.Val351Ile)	SIGLEC10 (V351I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489339	NM_033130.5(SIGLEC10):c.191T>C (p.Val64Ala)	SIGLEC10, SIGLEC10-AS1 (V64A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2485360	NM_033130.5(SIGLEC10):c.1301A>G (p.Gln434Arg)	SIGLEC10 (Q376R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477725	NM_033130.5(SIGLEC10):c.127T>C (p.Phe43Leu)	SIGLEC10, SIGLEC10-AS1 (F43L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2468986	NM_033130.5(SIGLEC10):c.2006C>T (p.Thr669Met)	SIGLEC10 (T574M +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463866	NM_033130.5(SIGLEC10):c.1258G>A (p.Glu420Lys)	SIGLEC10 (E272K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409198	NM_033130.5(SIGLEC10):c.71G>A (p.Arg24Gln)	SIGLEC10, SIGLEC10-AS1 (R24Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2388065	NM_033130.5(SIGLEC10):c.1931C>T (p.Pro644Leu)	SIGLEC10 (P549L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387416	NM_033130.5(SIGLEC10):c.1637C>T (p.Thr546Met)	SIGLEC10 (T393M +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382536	NM_033130.5(SIGLEC10):c.1129T>C (p.Cys377Arg)	SIGLEC10 (C319R +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2358971	NM_033130.5(SIGLEC10):c.1097C>T (p.Thr366Met)	SIGLEC10 (T276M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334546	NM_033130.5(SIGLEC10):c.668G>C (p.Gly223Ala)	SIGLEC10, SIGLEC10-AS1 (G175A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319906	NM_033130.5(SIGLEC10):c.53A>G (p.Asp18Gly)	SIGLEC10, SIGLEC10-AS1 (D18G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2306823	NM_033130.5(SIGLEC10):c.466C>T (p.Pro156Ser)	SIGLEC10, SIGLEC10-AS1 (P156S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284965	NM_033130.5(SIGLEC10):c.1861C>G (p.Arg621Gly)	SIGLEC10 (R436G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267967	NM_033130.5(SIGLEC10):c.268T>C (p.Phe90Leu)	SIGLEC10, SIGLEC10-AS1 (F90L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2267444	NM_033130.5(SIGLEC10):c.491G>T (p.Cys164Phe)	SIGLEC10, SIGLEC10-AS1 (C164F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264011	NM_033130.5(SIGLEC10):c.1960C>G (p.Gln654Glu)	SIGLEC10 (Q596E +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217440	NM_033130.5(SIGLEC10):c.1847C>A (p.Thr616Lys)	SIGLEC10 (T473K +6 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2210947	NM_033130.5(SIGLEC10):c.26C>T (p.Ser9Leu)	SIGLEC10, SIGLEC10-AS1 (S9L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2206794	NM_033130.5(SIGLEC10):c.1822G>A (p.Ala608Thr)	SIGLEC10 (A365T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205962	NM_033130.5(SIGLEC10):c.152C>T (p.Thr51Ile)	SIGLEC10, SIGLEC10-AS1 (T51I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 1526670	GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438)	FPR3, ZNF577 +115 more	Copy number gain	not specified	GLikely pathogenic
Select item 1340619	GRCh37/hg19 19q13.41(chr19:51769834-52415762)x3	CEACAM18, CLDND2 +21 more	Copy number gain	not provided	GUncertain significance
Select item 980768	GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	FLT3LG, FPR1 +308 more	Copy number gain	not provided	GPathogenic
Select item 972980	GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871)	FUZ, GARIN5A +228 more	Copy number gain	not provided	Gnot provided
Select item 816089	GRCh37/hg19 19q13.33-13.41(chr19:50469730-51916485)x3	ACP4, ASPDH +46 more	Copy number gain	not provided	GUncertain significance
Select item 816084	GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	CLDND2, IGSF23 +293 more	Copy number gain	not provided	GPathogenic
Select item 790210	NM_033130.5(SIGLEC10):c.1808C>A (p.Thr603Lys)	SIGLEC10 (T360K +6 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 775584	NM_033130.5(SIGLEC10):c.422-6T>C	SIGLEC10, SIGLEC10-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 774962	NM_033130.5(SIGLEC10):c.1779G>A (p.Thr593=)	SIGLEC10	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 773360	NM_033130.5(SIGLEC10):c.628A>G (p.Asn210Asp)	SIGLEC10, SIGLEC10-AS1 (N210D +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 770811	NM_033130.5(SIGLEC10):c.1605G>C (p.Leu535=)	SIGLEC10	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 769046	NM_033130.5(SIGLEC10):c.144= (p.Gln48=)	SIGLEC10, SIGLEC10-AS1	Variation (non-coding transcript variant +1 more)	not provided	GBenign
Select item 723714	NM_033130.5(SIGLEC10):c.561C>T (p.Ser187=)	SIGLEC10, SIGLEC10-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 710149	NM_033130.5(SIGLEC10):c.1290A>T (p.Pro430=)	SIGLEC10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 155383	GRCh38/hg38 19q13.41(chr19:51202361-51993020)x3	C19orf84, CD33 +62 more	Copy number gain	See cases	GUncertain significance
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	A1BG, A1BG-AS1 +782 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	MIR10394, MIR125A +806 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064933, LOC130064934 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	ZBTB45, ZFP28 +1081 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LILRA4, LILRA5 +761 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 68