Related gene-specific medical variations for Gene (Select 11281) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062951	GRCh37/hg19 7p14.1(chr7:39481317-39511176)x1	POU6F2	Copy number loss	not specified	GUncertain significance
Select item 443914	GRCh37/hg19 7p14.1(chr7:38984924-39087537)x3	POU6F2	Copy number gain	See cases	GUncertain significance
Select item 442581	GRCh37/hg19 7p14.1(chr7:39040397-39277606)x1	POU6F2	Copy number loss	See cases	GUncertain significance
Select item 442220	GRCh37/hg19 7p14.1(chr7:39326890-39398875)x3	POU6F2	Copy number gain	See cases	GUncertain significance

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