ZNF37A[gene] - ClinVar

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

Search results

Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	LOC130003254, LOC130003255 +1221 more	Copy number gain	See cases	GBenign
Select item 146088	GRCh38/hg38 10p11.22-11.1(chr10:31999920-38119681)x3	ANKRD30A, CCDC7 +119 more	Copy number gain	See cases	GPathogenic
Select item 152173	GRCh38/hg38 10p11.1(chr10:38052840-38766476)x4	LINC00999, LOC130003698 +2 more	Copy number gain	See cases	GUncertain significance
Select item 2477735	NM_001324250.3(ZNF37A):c.195G>T (p.Glu65Asp)	ZNF37A (E65D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493755	NM_001324250.3(ZNF37A):c.253A>G (p.Ser85Gly)	ZNF37A (S85G)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2318041	NM_001324250.3(ZNF37A):c.283G>A (p.Glu95Lys)	ZNF37A (E95K)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2619970	NM_001324250.3(ZNF37A):c.329T>A (p.Ile110Lys)	ZNF37A (I110K)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2517697	NM_001324250.3(ZNF37A):c.379T>G (p.Phe127Val)	ZNF37A (F127V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2552554	NM_001324250.3(ZNF37A):c.431A>G (p.Gln144Arg)	ZNF37A (Q144R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2270040	NM_001324250.3(ZNF37A):c.611A>T (p.Glu204Val)	ZNF37A (E204V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2408454	NM_001324250.3(ZNF37A):c.734A>G (p.Tyr245Cys)	ZNF37A (Y245C)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2545696	NM_001324250.3(ZNF37A):c.746G>A (p.Gly249Glu)	ZNF37A (G249E)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2494694	NM_001324250.3(ZNF37A):c.883G>C (p.Gly295Arg)	ZNF37A (G295R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2489767	NM_001324250.3(ZNF37A):c.893C>G (p.Pro298Arg)	ZNF37A (P298R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2550254	NM_001324250.3(ZNF37A):c.1115T>C (p.Val372Ala)	ZNF37A (V372A)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2299576	NM_001324250.3(ZNF37A):c.1177C>G (p.Leu393Val)	ZNF37A (L393V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2514504	NM_001324250.3(ZNF37A):c.1217C>T (p.Thr406Ile)	ZNF37A (T406I)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2540632	NM_001324250.3(ZNF37A):c.1288C>A (p.Leu430Ile)	ZNF37A (L430I)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2346186	NM_001324250.3(ZNF37A):c.1349A>G (p.Tyr450Cys)	ZNF37A (Y450C)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2407359	NM_001324250.3(ZNF37A):c.1352A>T (p.Tyr451Phe)	ZNF37A (Y451F)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2471948	NM_001324250.3(ZNF37A):c.1364C>T (p.Thr455Ile)	ZNF37A (T455I)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2362585	NM_001324250.3(ZNF37A):c.1430G>A (p.Arg477His)	ZNF37A (R477H)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2259556	NM_001324250.3(ZNF37A):c.1484A>G (p.Tyr495Cys)	ZNF37A (Y495C)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2621406	NM_001324250.3(ZNF37A):c.1541A>G (p.His514Arg)	ZNF37A (H514R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 155664	GRCh38/hg38 10p11.1(chr10:38140648-38777664)x3	LINC00999, ZNF37A	Copy number gain	See cases	GUncertain significance
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	MTG1, NPS +679 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	A1CF, ABCC2 +670 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 1527582	GRCh37/hg19 10p11.21-11.1(chr10:37697888-38677334)	MTRNR2L7, ZNF248 +3 more	Copy number gain	not specified	GUncertain significance
Select item 1339781	GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	ACBD7, ABI1 +180 more	Copy number gain	Mosaic supernumerary isodicentric chromosome 10	Gnot provided
Select item 815339	GRCh37/hg19 10p11.1(chr10:38064033-38900673)x3	ZNF37A, ZNF248 +2 more	Copy number gain	not provided	GLikely benign
Select item 815338	GRCh37/hg19 10p11.21-11.1(chr10:37189335-38900673)x3	ZNF37A, ZNF25 +4 more	Copy number gain	not provided	GLikely benign
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 563782	GRCh37/hg19 10p11.21-11.1(chr10:36797203-38900673)x3	MTRNR2L7, ANKRD30A +4 more	Copy number gain	not provided	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)	A1CF, ABCC2 +722 more	Copy number gain	See cases	GPathogenic
Select item 441986	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	NFKB2, NHLRC2 +722 more	Copy number gain	See cases	GPathogenic
Select item 393995	GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	A1CF, ANXA8L1 +723 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 37