Related gene-specific medical variations for Gene (Select 29091) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 980478	GRCh37/hg19 14q12(chr14:25344055-26769914)x3	STXBP6	Copy number gain	not provided	GUncertain significance
Select item 980476	GRCh37/hg19 14q12(chr14:25496337-26608460)x3	STXBP6	Copy number gain	not provided	GLikely benign
Select item 688882	GRCh37/hg19 14q12(chr14:25355269-26856647)x3	STXBP6	Copy number gain	not provided	GUncertain significance
Select item 687257	GRCh37/hg19 14q12(chr14:25292455-25431391)x3	STXBP6	Copy number gain	not provided	GUncertain significance

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