ClinVar for Gene (Select 92285) - ClinVar

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Links from Gene

Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258801	NM_152279.4(ZNF585B):c.628G>A (p.Gly210Arg)	ZNF585B (G210R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258800	NM_152279.4(ZNF585B):c.278G>A (p.Arg93His)	ZNF585B (R93H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3196970	NM_152279.4(ZNF585B):c.979A>G (p.Ile327Val)	ZNF585B (I327V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196969	NM_152279.4(ZNF585B):c.93T>G (p.Asp31Glu)	ZNF585B (D31E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196968	NM_152279.4(ZNF585B):c.906C>G (p.Asn302Lys)	ZNF585B (N302K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196967	NM_152279.4(ZNF585B):c.886A>G (p.Lys296Glu)	ZNF585B (K296E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196966	NM_152279.4(ZNF585B):c.866G>A (p.Arg289Gln)	ZNF585B (R289Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196965	NM_152279.4(ZNF585B):c.80T>C (p.Val27Ala)	ZNF585B (V27A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196964	NM_152279.4(ZNF585B):c.58G>A (p.Gly20Ser)	ZNF585B (G20S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196963	NM_152279.4(ZNF585B):c.547G>C (p.Glu183Gln)	ZNF585B (E183Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196962	NM_152279.4(ZNF585B):c.509A>G (p.Lys170Arg)	ZNF585B (K170R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196961	NM_152279.4(ZNF585B):c.405T>G (p.Phe135Leu)	ZNF585B (F135L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196960	NM_152279.4(ZNF585B):c.250C>T (p.Pro84Ser)	ZNF585B (P84S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196959	NM_152279.4(ZNF585B):c.217C>G (p.Pro73Ala)	ZNF585B (P73A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196958	NM_152279.4(ZNF585B):c.2155G>A (p.Val719Met)	ZNF585B (V719M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196957	NM_152279.4(ZNF585B):c.1518G>T (p.Arg506Ser)	ZNF585B (R506S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062386	GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3	SLC7A9, SNRPA +215 more	Copy number gain	not specified	GPathogenic
Select item 2685636	GRCh37/hg19 19q13.12(chr19:36804753-37720742)x1	ZFP14, ZFP82 +15 more	Copy number loss	not provided	GUncertain significance
Select item 2649770	NM_152279.4(ZNF585B):c.129C>T (p.His43=)	ZNF585B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649769	NM_152279.4(ZNF585B):c.2286T>C (p.Ser762=)	ZNF585B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2618940	NM_152279.4(ZNF585B):c.1000G>T (p.Val334Phe)	ZNF585B (V334F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617432	NM_152279.4(ZNF585B):c.391G>A (p.Glu131Lys)	ZNF585B (E131K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605736	NM_152279.4(ZNF585B):c.1173C>G (p.Phe391Leu)	ZNF585B (F391L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562082	NM_152279.4(ZNF585B):c.1397A>T (p.Tyr466Phe)	ZNF585B (Y466F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540283	NM_152279.4(ZNF585B):c.277C>T (p.Arg93Cys)	ZNF585B (R93C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511776	NM_152279.4(ZNF585B):c.455C>A (p.Pro152His)	ZNF585B (P152H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2508845	NM_152279.4(ZNF585B):c.526C>T (p.His176Tyr)	ZNF585B (H176Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454586	NM_152279.4(ZNF585B):c.1766G>A (p.Arg589His)	ZNF585B (R589H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412534	NM_152279.4(ZNF585B):c.1432C>T (p.Arg478Trp)	ZNF585B (R478W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403753	NM_152279.4(ZNF585B):c.26A>G (p.Gln9Arg)	ZNF585B (Q9R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403612	NM_152279.4(ZNF585B):c.748G>A (p.Ala250Thr)	ZNF585B (A250T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395639	NM_152279.4(ZNF585B):c.1741A>C (p.Thr581Pro)	ZNF585B (T581P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384631	NM_152279.4(ZNF585B):c.1279A>G (p.Thr427Ala)	ZNF585B (T427A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2372769	NM_152279.4(ZNF585B):c.774G>C (p.Lys258Asn)	ZNF585B (K258N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363250	NM_152279.4(ZNF585B):c.2266G>A (p.Val756Ile)	ZNF585B (V756I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362378	NM_152279.4(ZNF585B):c.1765C>T (p.Arg589Cys)	ZNF585B (R589C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361005	NM_152279.4(ZNF585B):c.2305G>A (p.Ala769Thr)	ZNF585B (A769T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2319335	NM_152279.4(ZNF585B):c.649A>C (p.Ser217Arg)	ZNF585B (S217R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297645	NM_152279.4(ZNF585B):c.1483A>G (p.Ile495Val)	ZNF585B (I495V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292132	NM_152279.4(ZNF585B):c.1918G>A (p.Gly640Arg)	ZNF585B (G640R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291025	NM_152279.4(ZNF585B):c.1316A>C (p.Lys439Thr)	ZNF585B (K439T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275411	NM_152279.4(ZNF585B):c.371A>T (p.Tyr124Phe)	ZNF585B (Y124F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235293	NM_152279.4(ZNF585B):c.469C>T (p.Leu157Phe)	ZNF585B (L157F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228923	NM_152279.4(ZNF585B):c.953G>A (p.Arg318His)	ZNF585B (R318H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1807905	GRCh37/hg19 19q13.12-13.13(chr19:37389799-38562489)x3	SIPA1L3, WDR87 +17 more	Copy number gain	not provided	GUncertain significance
Select item 1526662	GRCh37/hg19 19q13.12(chr19:36910874-37705345)	ZNF260, ZNF345 +12 more	Copy number loss	not specified	GUncertain significance
Select item 1330177	GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	ACP7, ACTMAP +255 more	Copy number gain	Specific learning disability	GPathogenic
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 more	Copy number gain	not provided	GPathogenic
Select item 625760	GRCh37/hg19 19q13.11-13.12(chr19:35111811-37744992)	ALKBH6, APLP1 +79 more	Copy number loss	Generalized epilepsy with febrile seizures plus, type 1	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 442455	GRCh37/hg19 19q13.12(chr19:37431411-37747108)x1	ZNF383, ZNF420 +3 more	Copy number loss	See cases	GUncertain significance
Select item 253766	GRCh37/hg19 19q13.12-13.13(chr19:36475577-38399402)x3	SIPA1L3, ALKBH6 +41 more	Copy number gain	See cases	GUncertain significance
Select item 253452	GRCh37/hg19 19q13.12-13.2(chr19:37582250-41630908)x3	DPF1, DYRK1B +105 more	Copy number gain	See cases	GPathogenic
Select item 221401	GRCh37/hg19 19q13.12-13.2(chr19:36685995-38708166)x1	DPF1, SIPA1L3 +31 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221351	chr19:36674305-38652962 complex variant	SIPA1L3, WDR87 +30 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 153332	GRCh38/hg38 19q13.12(chr19:37107396-37679721)x1	LINC01535, LOC112543487 +28 more	Copy number loss	See cases	GUncertain significance
Select item 147631	GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1	ALKBH6, ANKRD27 +439 more	Copy number loss	See cases	GPathogenic
Select item 146619	GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1	ALKBH6, ANKRD27 +459 more	Copy number loss	See cases	GPathogenic
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 60