ClinVar for Gene (Select 101927967) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154484	GRCh38/hg38 2p12(chr2:77120615-77959416)x3	LINC01851, LOC101927967 +2 more	Copy number gain	See cases	GUncertain significance
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	LOC126806252, LOC126806253 +2457 more	Copy number gain	See cases	GBenign
Select item 150901	GRCh38/hg38 2p12(chr2:77820412-78374887)x1	LINC01851, LOC101927948 +4 more	Copy number loss	See cases	GLikely benign
Select item 150241	GRCh38/hg38 2p12(chr2:78202871-79113257)x3	LOC101927967, LOC105374820 +3 more	Copy number gain	See cases	GLikely benign
Select item 146814	GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3	AAK1, ACTG2 +768 more	Copy number gain	See cases	GPathogenic
Select item 145403	GRCh38/hg38 2p12-11.2(chr2:77025216-90282666)x3	ATOH8, C2orf68 +302 more	Copy number gain	See cases	GPathogenic

ClinVar