Related gene-specific medical variations for Gene (Select 100128260) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 441906	GRCh37/hg19 Yq12(chrY:59033287-59363566)x0	WASIR1	Copy number loss	See cases	GBenign
Select item 395451	GRCh37/hg19 Xq28(chrX:154933719-155246585)x0	WASIR1	Copy number loss	See cases	GBenign
Select item 395040	GRCh37/hg19 Yq12(chrY:59036725-59349591)x0	WASIR1	Copy number loss	See cases	GBenign
Select item 394686	GRCh37/hg19 Xq28(chrX:155236606-155246585)x3	WASIR1	Copy number gain	See cases	GBenign
Select item 394364	GRCh37/hg19 Yq12(chrY:59028692-59349591)x0	WASIR1	Copy number loss	See cases	GBenign
Select item 394276	GRCh37/hg19 Yq12(chrY:58983344-59358798)x0	WASIR1	Copy number loss	See cases	GBenign

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