ZNF32[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	ABI1, ACBD5 +1221 more	Copy number gain	See cases	GBenign
Select item 154900	GRCh38/hg38 10q11.21-21.3(chr10:42112187-67400675)x3	A1CF, ADO +561 more	Copy number gain	See cases	GPathogenic
Select item 145479	GRCh38/hg38 10q11.21-11.23(chr10:42395201-50877059)x3	LOC130003758, LOC130003759 +309 more	Copy number gain	See cases	GPathogenic
Select item 145481	GRCh38/hg38 10q11.21-22.2(chr10:42685306-73715908)x3	A1CF, ADAMTS14 +902 more	Copy number gain	See cases	GPathogenic
Select item 144977	GRCh38/hg38 10q11.21-21.1(chr10:42884294-52265317)x3	FAM170B, FAM170B-AS1 +306 more	Copy number gain	See cases	GPathogenic
Select item 2623044	NM_006973.3(ZNF32):c.669G>T (p.Arg223Ser)	ZNF32, ZNF32-AS1 +1 more (R227S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619969	NM_006973.3(ZNF32):c.623T>C (p.Ile208Thr)	ZNF32, ZNF32-AS1 +1 more (I183T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640420	NM_006973.3(ZNF32):c.622A>G (p.Ile208Val)	ZNF32, ZNF32-AS1 +1 more (I183V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2546332	NM_006973.3(ZNF32):c.604G>A (p.Gly202Arg)	ZNF32, ZNF32-AS1 +1 more (G202R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195124	NM_006973.3(ZNF32):c.484G>A (p.Glu162Lys)	ZNF32, ZNF32-AS1 +1 more (E137K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369630	NM_006973.3(ZNF32):c.454G>A (p.Glu152Lys)	ZNF32, ZNF32-AS1 +1 more (E127K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195123	NM_006973.3(ZNF32):c.346G>A (p.Ala116Thr)	ZNF32, ZNF32-AS1 +1 more (A116T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3195122	NM_006973.3(ZNF32):c.318G>T (p.Glu106Asp)	ZNF32, ZNF32-AS1 +1 more (E81D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217027	NM_006973.3(ZNF32):c.278C>T (p.Thr93Met)	ZNF32, ZNF32-AS1 +1 more (T93M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207596	NM_006973.3(ZNF32):c.260G>A (p.Arg87Gln)	ZNF32, ZNF32-AS1 +1 more (R91Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316598	NM_006973.3(ZNF32):c.259C>T (p.Arg87Trp)	ZNF32, ZNF32-AS1 +1 more (R91W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381513	NM_006973.3(ZNF32):c.221A>G (p.Gln74Arg)	ZNF32, ZNF32-AS1 +1 more (Q78R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363242	NM_006973.3(ZNF32):c.89A>G (p.His30Arg)	ZNF32, ZNF32-AS1 +1 more (H34R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684602	GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3	RRP12, RTKN2 +332 more	Copy number gain	not provided	GPathogenic
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 1527583	GRCh37/hg19 10q11.21(chr10:43683704-44151599)	FXYD4, HNRNPF +4 more	Copy number gain	not specified	GUncertain significance
Select item 1339781	GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	ARL5B, LARP4B +180 more	Copy number gain	Mosaic supernumerary isodicentric chromosome 10	Gnot provided
Select item 624469	GRCh37/hg19 10p11.21-q11.22(chr10:37149872-46169876)x3	ALOX5, ANKRD30A +24 more	Copy number gain	not provided	GLikely pathogenic
Select item 523165	GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1	COX15, CPEB3 +569 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 495230	NC_000010.10:g.43611191_61663279inv	CCDC6, ZNF32 +75 more	Inversion	Pediatric metastatic thyroid tumour	GLikely pathogenic
Select item 443388	GRCh37/hg19 10q11.21(chr10:42706947-44489498)x3	BMS1, CSGALNACT2 +8 more	Copy number gain	See cases	GUncertain significance
Select item 443260	GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	ABI1, ACBD5 +205 more	Copy number gain	See cases	GPathogenic
Select item 441987	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	INA, INPP5A +721 more	Copy number gain	See cases	GPathogenic
Select item 441986	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	A1CF, ABCC2 +721 more	Copy number gain	See cases	GPathogenic
Select item 393995	GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	A1CF, ABCC2 +722 more	Copy number gain	See cases	GPathogenic

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Items: 31