ClinVar for Gene (Select 122757931) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155615	GRCh38/hg38 2p25.3-21(chr2:236816-45983232)x3	LINC01115, LINC01121 +1400 more	Copy number gain	See cases	GPathogenic
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 152534	GRCh38/hg38 2p21(chr2:45192069-45734384)x3	LINC01121, LOC112840936 +13 more	Copy number gain	See cases	GLikely benign
Select item 151412	GRCh38/hg38 2p21(chr2:45253291-45851241)x3	LINC01121, LOC112840936 +21 more	Copy number gain	See cases	GLikely benign
Select item 149908	GRCh38/hg38 2p21(chr2:45273355-45734463)x3	LOC112840936, LOC122757931 +12 more	Copy number gain	See cases	GLikely benign
Select item 144278	GRCh38/hg38 2p21(chr2:44942723-45431847)x3	LINC01121, LOC122757931 +6 more	Copy number gain	See cases	GUncertain significance
Select item 59143	GRCh38/hg38 2p22.1-16.1(chr2:40738282-57863821)x3	ABCG5, ABCG8 +443 more	Copy number gain	See cases	GPathogenic
Select item 59133	GRCh38/hg38 2p25.3-16.1(chr2:66097-55570637)x3	LOC129933311, LOC129933312 +1631 more	Copy number gain	See cases	GPathogenic

ClinVar