"Baylor Genetics"[submitter] AND "SLC9A3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1034058	NM_004174.4(SLC9A3):c.1862A>G (p.Gln621Arg)	SLC9A3, SLC9A3-AS1 (Q612R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 625702	GRCh37/hg19 5p15.33-15.31(chr5:140474-9792158)	ADAMTS16, ADCY2 +40 more	Copy number loss	5p partial monosomy syndrome	GPathogenic
Select item 625701	GRCh37/hg19 5p15.33-14.1(chr5:140474-26906925)	ADAMTS16, ADCY2 +67 more	Copy number loss	5p partial monosomy syndrome	GPathogenic

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