"ISCA site 2"[submitter] AND "LINC01237"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 147844	GRCh38/hg38 2q37.2-37.3(chr2:235028429-242066108)x1	ACKR3, AGAP1 +314 more	Copy number loss	See cases	GPathogenic
Select item 153010	GRCh38/hg38 2q37.3(chr2:241910415-242065208)x1	LINC01237, LINC01238 +4 more	Copy number loss	See cases	GBenign
Select item 148169	GRCh38/hg38 2q37.3(chr2:241914437-242066108)x1	LINC01237, LINC01238 +4 more	Copy number loss	See cases	GBenign
Select item 144410	GRCh38/hg38 2q37.3(chr2:241914437-242065208)x1	LINC01237, LINC01238 +4 more	Copy number loss	See cases	GBenign
Select item 144409	GRCh38/hg38 2q37.3(chr2:241914437-242065208)x3	LINC01237, LINC01238 +4 more	Copy number gain	See cases	GBenign
Select item 144401	GRCh38/hg38 2q37.3(chr2:241981907-242005889)x1	LINC01237, LOC132205954 +1 more	Copy number loss	See cases	GBenign

ClinVar