ClinVar for MedGen (Select 868596) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 870524	GRCh37/hg19 Yp11.31(chrY:2650140-2777517)x1	RPS4Y1, SRY	Copy number gain	Sex reversal	GPathogenic
Select item 870523	GRCh37/hg19 Yp11.31-11.2(chrY:2650140-6367818)x1	FAM197Y9, PCDH11Y +11 more	Copy number gain	Sex reversal	GPathogenic
Select item 870517	GRCh37/hg19 Yp11.31-11.2(chrY:2650140-7019586)x1	AMELY, FAM197Y9 +13 more	Copy number gain	Sex reversal	GPathogenic
Select item 870516	GRCh37/hg19 Yp11.31-11.2(chrY:2650140-6172892)x1	FAM197Y9, PCDH11Y +6 more	Copy number gain	Sex reversal	GPathogenic

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