ClinVar for Gene (Select 101927994) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154056	GRCh38/hg38 2q21.1-21.2(chr2:131291207-132406186)x3	ANKRD30BL, C2orf27A +24 more	Copy number gain	See cases	GLikely benign
Select item 152948	GRCh38/hg38 2q21.1-21.2(chr2:131100857-132436431)x3	LINC01120, LINC01945 +32 more	Copy number gain	See cases	GUncertain significance
Select item 151118	GRCh38/hg38 2q21.1-21.2(chr2:131409034-131940119)x1	C2orf27A, CCDC74A +14 more	Copy number loss	See cases	GUncertain significance
Select item 150720	GRCh38/hg38 2q21.1(chr2:131340404-131643336)x1	CCDC74A, LINC01087 +11 more	Copy number loss	See cases	GLikely benign
Select item 150449	GRCh38/hg38 2q21.1-21.2(chr2:131451345-131736366)x1	C2orf27A, CCDC74A +13 more	Copy number loss	See cases	GLikely benign
Select item 150443	GRCh38/hg38 2q21.1-21.2(chr2:131451345-131736366)x3	C2orf27A, CCDC74A +13 more	Copy number gain	See cases	GLikely benign
Select item 147544	GRCh38/hg38 2q14.3-22.1(chr2:123445762-140592538)x1	ACMSD, AMER3 +336 more	Copy number loss	See cases	GPathogenic
Select item 60184	GRCh38/hg38 2q14.1-21.3(chr2:118086324-134964738)x1	ACMSD, AMER3 +391 more	Copy number loss	See cases	GPathogenic

ClinVar