Related gene-specific medical variations for Gene (Select 22829) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689591	NM_001365588.1(NLGN4Y):c.1672C>T (p.Gln558Ter)	NLGN4Y (Q370* +2 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1809239	GRCh37/hg19 Yq11.221(chrY:16877505-17348784)x4	NLGN4Y	Copy number gain	not provided	GUncertain significance
Select item 816439	GRCh37/hg19 Yq11.221(chrY:16554396-16878467)x2	NLGN4Y	Copy number gain	not provided	GUncertain significance
Select item 687222	GRCh37/hg19 Yq11.221(chrY:16230512-16646954)x2	NLGN4Y	Copy number gain	not provided	GUncertain significance
Select item 559565	NM_001365588.1(NLGN4Y):c.260G>A (p.Arg87Gln)	NLGN4Y (R87Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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