dbVar for Gene (Select 2589) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	LOC100420948, NPM1P2, 941 more genes
nsv3924638	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402	HMGN1P30, LOC107985134, 596 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	MIX23P1, LOC105372087, 942 more genes
nsv3923838	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381	WDR7-OT1, HMGN1P30, 941 more genes
nsv3921154	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr18: 30,288,042-31,589,339 , GRCh38 chr18: 34,454,080-35,755,377 , GRCh37 chr18: 32,034,044-33,335,341	MAPRE2, LOC105372065, 14 more genes
nsv3920818	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298	AQP4-AS1, SERPINB8, 670 more genes
nsv3920302	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 29,881,080-37,228,316 , GRCh38 chr18: 34,047,118-41,394,354 , GRCh37 chr18: 31,627,082-38,974,318	FHOD3, MIR3975, 61 more genes
nsv3919896	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 31,655,749-42,564,094 , NCBI36 chr18: 27,489,710-38,398,057 , GRCh37 chr18: 29,235,712-40,144,059	LOC107985168, NRBF2P1, 100 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	LIVAR, LINC03069, 941 more genes
nsv3918717	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 35,097,761-39,379,288 , NCBI36 chr18: 30,931,723-35,213,250 , GRCh37 chr18: 32,677,725-36,959,252	LOC105372065, LOC105372068, 45 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	LOC105372027, ASXL3, 945 more genes
nsv3916426	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391	TPGS2, TWSG1-DT, 941 more genes
nsv3916358	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 20,941,324-40,360,620 , NCBI36 chr18: 16,775,283-36,194,582 , GRCh37 chr18: 18,521,285-37,940,584	MIR4741, LOC105372029, 220 more genes
nsv3915938	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 18,569,723-77,967,869 , GRCh38 chr18: 20,989,762-80,209,986 , NCBI36 chr18: 16,823,721-76,068,860	LOC105372061, LOC107985171, 670 more genes
nsv3913779	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr18: 29,207,760-33,198,709 , GRCh37 chr18: 30,953,762-34,944,711 , GRCh38 chr18: 33,373,798-37,364,748	DTNA, GALNT1, 36 more genes
nsv3912925	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,111,023 , GRCh38 chr18: 148,963-80,252,149 , GRCh37 chr18: 148,963-78,010,032	LOC105372038, RN7SKP182, 941 more genes
nsv3912888	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 27,024,475-37,983,616 , NCBI36 chr18: 25,278,473-36,237,614 , GRCh38 chr18: 29,444,510-40,403,652	KLHL14, ZNF271P, 107 more genes
nsv3912224	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 27,945,491-39,904,182 , GRCh38 chr18: 32,111,530-44,070,219 , GRCh37 chr18: 29,691,493-41,650,184	SYT4, MIR4318, 94 more genes
nsv3911956	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 27,957,066-76,111,023 , GRCh38 chr18: 32,123,105-80,252,149 , GRCh37 chr18: 29,703,068-78,010,032	RPL7AP66, GLUD1P4, 526 more genes
nsv3911404	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 16,794,279-76,093,303 , GRCh38 chr18: 20,960,320-80,234,429 , GRCh37 chr18: 18,540,281-77,992,312	LOC107985178, RN7SL310P, 670 more genes

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Number of Variants: 20

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Organism

Variant Type

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 253

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Number of Variants: 20

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