"GeneDx"[submitter] AND "ADAMTS9-AS2"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1277022	NM_182920.2(ADAMTS9):c.286T>A (p.Ser96Thr)	ADAMTS9, ADAMTS9-AS2 (S96T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1263244	NM_182920.2(ADAMTS9):c.116-80C>G	ADAMTS9, ADAMTS9-AS2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 57772	GRCh38/hg38 3p14.1-12.3(chr3:64761248-78410098)x1	ADAMTS9-AS2, ARL6IP5 +234 more	Copy number loss	See cases	GPathogenic

Format

Sort by

Choose Destination