"ISCA site 4"[submitter] AND "CHL1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57397	GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3	LOC129936421, LOC129936422 +962 more	Copy number gain	See cases	GPathogenic
Select item 150281	GRCh38/hg38 3p26.3-25.3(chr3:52747-8370373)x1	ARL8B, BHLHE40 +141 more	Copy number loss	See cases	GPathogenic
Select item 56999	GRCh38/hg38 3p26.3(chr3:76052-229025)x1	CHL1, CHL1-AS2 +2 more	Copy number loss	See cases	GUncertain significance
Select item 144261	GRCh38/hg38 3p26.3(chr3:190813-1155998)x1	CHL1, CHL1-AS1 +5 more	Copy number loss	See cases	GUncertain significance
Select item 154926	GRCh38/hg38 3p26.3(chr3:199392-338596)x3	CHL1, LOC111429626	Copy number gain	See cases	GUncertain significance
Select item 150012	GRCh38/hg38 3p26.3(chr3:199392-241339)x1	CHL1	Copy number loss	See cases	GUncertain significance
Select item 146795	GRCh38/hg38 3p26.3(chr3:228954-241339)x1	CHL1	Copy number loss	See cases	Gconflicting data from submitters
Select item 150956	GRCh38/hg38 3p26.3(chr3:244643-270432)x1	CHL1, LOC111429626	Copy number loss	See cases	GLikely benign
Select item 144344	GRCh38/hg38 3p26.3(chr3:401550-1091944)x3	CHL1, LINC01266 +1 more	Copy number gain	See cases	GUncertain significance

ClinVar