ClinVar for Gene (Select 124403954) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154900	GRCh38/hg38 10q11.21-21.3(chr10:42112187-67400675)x3	A1CF, ADO +561 more	Copy number gain	See cases	GPathogenic
Select item 154129	GRCh38/hg38 10q11.23-21.1(chr10:50453699-51121757)x3	A1CF, ASAH2B +22 more	Copy number gain	See cases	GUncertain significance
Select item 149970	GRCh38/hg38 10q11.23(chr10:49971505-50699223)x1	AGAP6, ASAH2 +32 more	Copy number loss	See cases	GUncertain significance
Select item 148407	GRCh38/hg38 10q11.23(chr10:50151274-50673230)x3	ASAH2, LOC124403953 +27 more	Copy number gain	See cases	GUncertain significance
Select item 145481	GRCh38/hg38 10q11.21-22.2(chr10:42685306-73715908)x3	A1CF, ADAMTS14 +902 more	Copy number gain	See cases	GPathogenic
Select item 145479	GRCh38/hg38 10q11.21-11.23(chr10:42395201-50877059)x3	LOC130003758, LOC130003759 +309 more	Copy number gain	See cases	GPathogenic
Select item 144977	GRCh38/hg38 10q11.21-21.1(chr10:42884294-52265317)x3	FAM170B, FAM170B-AS1 +306 more	Copy number gain	See cases	GPathogenic
Select item 58551	GRCh38/hg38 10q11.22-11.23(chr10:45931517-50655311)x1	AGAP6, AGAP9 +147 more	Copy number loss	See cases	GPathogenic

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