LOC124421499[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144515	GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3	CHID1, CHRNA10 +917 more	Copy number gain	See cases	GPathogenic
Select item 147607	GRCh38/hg38 11p15.4-15.2(chr11:9989516-16825806)x1	ADM, ADM-DT +208 more	Copy number loss	See cases	GPathogenic
Select item 146351	GRCh38/hg38 11p15.2(chr11:14619894-15179026)x3	CALCA, CALCB +14 more	Copy number gain	See cases	GUncertain significance
Select item 154135	GRCh38/hg38 11p15.2(chr11:14684722-15210307)x3	CALCA, CALCB +13 more	Copy number gain	See cases	GUncertain significance
Select item 151351	GRCh38/hg38 11p15.2(chr11:14914381-15240180)x3	CALCA, CALCB +7 more	Copy number gain	See cases	GLikely benign
Select item 57954	GRCh38/hg38 11p15.2(chr11:14924804-15253488)x3	CALCA, CALCB +7 more	Copy number gain	See cases	GUncertain significance

ClinVar