"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "C16orf9 - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 657383	NC_000016.10:g.(?_3727698)_(4802591_?)del	LINC01569, LINC02861 +66 more	Deletion	Rubinstein-Taybi syndrome	GPathogenic
Select item 771013	NM_001145011.2(C16orf96):c.1450C>T (p.Arg484Cys)	C16orf96 (R484C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2425098	NC_000016.9:g.(?_3293141)_(5971108_?)dup	CDIP1, CLUAP1 +45 more	Duplication	Rubinstein-Taybi syndrome	GUncertain significance
Select item 2425037	NC_000016.9:g.(?_256302)_(4852572_?)dup	ABCA3, ADCY9 +170 more	Duplication	Hyperaldosteronism, familial, type IV +3 more	GUncertain significance
Select item 831384	NC_000016.10:g.(?_3727698)_(4802591_?)dup	CORO7, ADCY9 +21 more	Duplication	Amelocerebrohypohidrotic syndrome	GUncertain significance

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