ClinVar for Gene (Select 101928031) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154594	GRCh38/hg38 2p11.2(chr2:83448114-83990562)x3	LINC01809, LOC115945162 +1 more	Copy number gain	See cases	GUncertain significance
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	HAAO, HADHA +2457 more	Copy number gain	See cases	GBenign
Select item 152528	GRCh38/hg38 2p11.2(chr2:83448114-84024195)x4	LINC01809, LOC115945162 +1 more	Copy number gain	See cases	GBenign
Select item 147362	GRCh38/hg38 2p11.2(chr2:83448114-83990562)x4	LINC01809, LOC115945162 +1 more	Copy number gain	See cases	GUncertain significance
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 145556	GRCh38/hg38 2p12-11.2(chr2:82224116-83882899)x1	LINC01809, LOC112841601 +4 more	Copy number loss	See cases	GLikely benign
Select item 145403	GRCh38/hg38 2p12-11.2(chr2:77025216-90282666)x3	ATOH8, C2orf68 +302 more	Copy number gain	See cases	GPathogenic

ClinVar