C14orf132[gene] and "single gene"[properties] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685498	GRCh37/hg19 14q32.2(chr14:96474952-96532029)x1	C14orf132	Copy number loss	not provided	GUncertain significance
Select item 815675	GRCh37/hg19 14q32.2(chr14:96453503-96589931)x1	C14orf132	Copy number loss	not provided	GLikely benign
Select item 395637	GRCh37/hg19 14q32.2(chr14:96490305-96558424)x1	C14orf132	Copy number loss	See cases	GUncertain significance

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