Related gene-specific medical variations for Gene (Select 54875) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980891	GRCh37/hg19 9p22.2(chr9:17053143-17185702)x1	CNTLN	Copy number loss	not provided	GLikely benign
Select item 815240	GRCh37/hg19 9p22.2(chr9:17350842-17419424)x1	CNTLN	Copy number loss	not provided	GLikely benign
Select item 442924	GRCh37/hg19 9p22.2(chr9:16931294-17138176)x1	CNTLN	Copy number loss	See cases	GUncertain significance

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