ZNF576[gene] - ClinVar

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

Search results

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 545227	Single allele	LOC130064626, LOC130064627 +215 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 60277	GRCh38/hg38 19q13.31(chr19:43338231-43853163)x3	PHLDB3, PINLYP +55 more	Copy number gain	See cases	GUncertain significance
Select item 3258754	NM_001145347.2(ZNF576):c.11C>A (p.Pro4Gln)	ZNF576 (P4Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348980	NM_001145347.2(ZNF576):c.32A>C (p.Lys11Thr)	ZNF576 (K11T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355973	NM_001145347.2(ZNF576):c.40G>T (p.Asp14Tyr)	ZNF576 (D14Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258752	NM_001145347.2(ZNF576):c.95G>A (p.Gly32Glu)	ZNF576 (G32E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604001	NM_001145347.2(ZNF576):c.272G>A (p.Arg91His)	ZNF576 (R91H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363305	NM_001145347.2(ZNF576):c.313A>G (p.Thr105Ala)	ZNF576 (T105A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246262	NM_001145347.2(ZNF576):c.323C>T (p.Ala108Val)	ZNF576 (A108V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258755	NM_001145347.2(ZNF576):c.373G>A (p.Val125Ile)	ZNF576 (V125I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315581	NM_001145347.2(ZNF576):c.399G>T (p.Met133Ile)	ZNF576 (M133I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487319	NM_001145347.2(ZNF576):c.409C>T (p.Arg137Cys)	ZNF576 (R137C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196890	NM_001145347.2(ZNF576):c.430G>A (p.Ala144Thr)	ZNF576 (A144T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349976	NM_001145347.2(ZNF576):c.491G>A (p.Arg164Gln)	ZNF576 (R164Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258753	NM_001145347.2(ZNF576):c.499C>T (p.Arg167Trp)	ZNF576 (R167W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	CADM4, CEACAM16 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 685142	GRCh37/hg19 19q13.31(chr19:43803157-44105375)x3	CD177, ETHE1 +9 more	Copy number gain	not provided	GUncertain significance
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	APOC1, APOC2 +120 more	Copy number loss	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: 22