Related gene-specific medical variations for Gene (Select 84075) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980487	GRCh37/hg19 14q21.2(chr14:44556606-44984689)x1	FSCB	Copy number loss	not provided	GLikely benign
Select item 815650	GRCh37/hg19 14q21.2(chr14:44750751-45024841)x1	FSCB	Copy number loss	not provided	GLikely benign
Select item 395500	GRCh37/hg19 14q21.2(chr14:44623010-45083670)x3	FSCB	Copy number gain	See cases	GLikely benign

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