ClinVar for Gene (Select 129936396) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153415	GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3	ACAA1, ACVR2B +1111 more	Copy number gain	See cases	GPathogenic
Select item 150437	GRCh38/hg38 3p24.1(chr3:28103194-29104771)x3	AZI2, CMC1 +11 more	Copy number gain	See cases	GLikely benign
Select item 150118	GRCh38/hg38 3p24.1(chr3:28426784-29104789)x3	LINC00693, LOC126806638 +3 more	Copy number gain	See cases	GUncertain significance
Select item 148942	GRCh38/hg38 3p26.3-24.1(chr3:32241-30064208)x3	ANKRD28, ARL8B +799 more	Copy number gain	See cases	GPathogenic
Select item 57978	GRCh38/hg38 3p25.3-22.2(chr3:11463328-38919543)x3	LOC132088948, LOC132088950 +730 more	Copy number gain	See cases	GPathogenic
Select item 57397	GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3	LOC129936421, LOC129936422 +962 more	Copy number gain	See cases	GPathogenic

ClinVar