ClinVar for Gene (Select 101060004) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154504	GRCh38/hg38 20q13.13(chr20:47858604-48480223)x1	LINC00494, LINC01522 +13 more	Copy number loss	See cases	GUncertain significance
Select item 151393	GRCh38/hg38 20q13.13(chr20:47865750-48502791)x3	LINC00494, LINC01522 +17 more	Copy number gain	See cases	GBenign
Select item 149315	GRCh38/hg38 20q13.13(chr20:47850027-48502835)x3	LINC00494, LINC01522 +20 more	Copy number gain	See cases	GLikely benign
Select item 148219	GRCh38/hg38 20q13.13(chr20:47810469-48502835)x3	LINC00494, LINC01522 +21 more	Copy number gain	See cases	GUncertain significance
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	JPH2, KAT14 +2522 more	Copy number gain	See cases	GPathogenic
Select item 146461	GRCh38/hg38 20q13.13(chr20:47858604-48480223)x3	LINC00494, LINC01522 +13 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 59218	GRCh38/hg38 20q13.12-13.33(chr20:44787704-64277321)x3	ABHD16B, ACOT8 +1024 more	Copy number gain	See cases	GPathogenic

ClinVar