Related gene-specific medical variations for Gene (Select 83869) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685029	GRCh37/hg19 Yq11.222(chrY:21039793-21294304)x3	TTTY14	Copy number gain	not provided	GUncertain significance
Select item 1341195	GRCh37/hg19 Yq11.222(chrY:21121159-21604486)x2	TTTY14	Copy number gain	not provided	GUncertain significance
Select item 395019	GRCh37/hg19 Yq11.222(chrY:21053353-21412851)x2	TTTY14	Copy number gain	See cases	GBenign
Select item 394620	GRCh37/hg19 Yq11.222(chrY:21053353-21251249)x2	TTTY14	Copy number gain	See cases	GLikely benign

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