Related gene-specific medical variations for Gene (Select 90655) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807872	GRCh37/hg19 Yp11.2(chrY:3182436-4765099)x0	TGIF2LY	Copy number loss	not provided	GUncertain significance
Select item 1341306	GRCh37/hg19 Yp11.2(chrY:3054478-3476941)x2	TGIF2LY	Copy number gain	not provided	GLikely benign
Select item 979248	GRCh37/hg19 Yp11.2(chrY:3147902-3476941)x2	TGIF2LY	Copy number gain	not provided	GUncertain significance
Select item 564951	GRCh37/hg19 Yp11.31-11.2(chrY:2915750-3476941)x2	TGIF2LY	Copy number gain	not provided	GUncertain significance

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