ClinVar for Gene (Select 130063302) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180341	NM_003811.4(TNFSF9):c.10G>A (p.Ala4Thr)	LOC130063302, TNFSF9 (A4T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380113	NM_003811.4(TNFSF9):c.16G>A (p.Asp6Asn)	LOC130063302, TNFSF9 (D6N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 154560	GRCh38/hg38 19p13.3(chr19:259395-6795611)x3	LOC130062978, LOC130062979 +903 more	Copy number gain	See cases	GPathogenic
Select item 150491	GRCh38/hg38 19p13.3-13.2(chr19:5905175-6916287)x3	ACER1, ACSBG2 +113 more	Copy number gain	See cases	GUncertain significance
Select item 59082	GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3	LOC130063254, LOC130063255 +810 more	Copy number gain	See cases	GPathogenic

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