ClinVar for Gene (Select 7539) - ClinVar

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Links from Gene

Items: 70

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334489	NM_003408.3(ZFP37):c.1396T>C (p.Cys466Arg)	ZFP37 (C481R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334487	NM_003408.3(ZFP37):c.1742C>A (p.Ala581Asp)	ZFP37 (A582D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334486	NM_003408.3(ZFP37):c.439G>C (p.Ala147Pro)	ZFP37 (A147P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334485	NM_003408.3(ZFP37):c.304T>C (p.Cys102Arg)	ZFP37 (C102R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334484	NM_003408.3(ZFP37):c.1735G>C (p.Glu579Gln)	ZFP37 (E579Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193147	NM_003408.3(ZFP37):c.443A>C (p.Lys148Thr)	ZFP37 (K148T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193146	NM_003408.3(ZFP37):c.362A>T (p.Asp121Val)	ZFP37 (D136V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193145	NM_003408.3(ZFP37):c.341C>T (p.Thr114Ile)	ZFP37 (T114I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193144	NM_003408.3(ZFP37):c.28C>A (p.Leu10Met)	LOC130002408, ZFP37 (L10M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193143	NM_003408.3(ZFP37):c.1750G>A (p.Ala584Thr)	ZFP37 (A599T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193141	NM_003408.3(ZFP37):c.1423C>T (p.His475Tyr)	ZFP37 (H476Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3193140	NM_003408.3(ZFP37):c.1225G>A (p.Glu409Lys)	ZFP37 (E409K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 2621514	NM_003408.3(ZFP37):c.1390A>G (p.Asn464Asp)	ZFP37 (N479D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555767	NM_003408.3(ZFP37):c.1340C>T (p.Ser447Phe)	ZFP37 (S447F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551092	NM_003408.3(ZFP37):c.756A>T (p.Leu252Phe)	ZFP37 (L252F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547920	NM_003408.3(ZFP37):c.1573G>A (p.Gly525Ser)	ZFP37 (G525S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542543	NM_003408.3(ZFP37):c.151C>T (p.Pro51Ser)	ZFP37 (P51S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507640	NM_003408.3(ZFP37):c.1481G>A (p.Cys494Tyr)	ZFP37 (C494Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485712	NM_003408.3(ZFP37):c.1388G>A (p.Cys463Tyr)	ZFP37 (C463Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480467	NM_003408.3(ZFP37):c.1088C>T (p.Ala363Val)	ZFP37 (A364V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461157	NM_003408.3(ZFP37):c.148G>C (p.Asp50His)	ZFP37 (D65H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407624	NM_003408.3(ZFP37):c.464G>C (p.Gly155Ala)	ZFP37 (G170A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377676	NM_003408.3(ZFP37):c.32C>G (p.Thr11Arg)	LOC130002408, ZFP37 (T11R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365621	NM_003408.3(ZFP37):c.1619C>T (p.Thr540Ile)	ZFP37 (T555I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335970	NM_003408.3(ZFP37):c.1505C>T (p.Ser502Leu)	ZFP37 (S503L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333856	NM_003408.3(ZFP37):c.1769T>C (p.Ile590Thr)	ZFP37 (I590T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331410	NM_003408.3(ZFP37):c.1538G>A (p.Gly513Asp)	ZFP37 (G514D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330373	NM_003408.3(ZFP37):c.1648T>C (p.Cys550Arg)	ZFP37 (C550R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327402	NM_003408.3(ZFP37):c.1328A>G (p.Lys443Arg)	ZFP37 (K443R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302445	NM_003408.3(ZFP37):c.1778G>A (p.Arg593Gln)	ZFP37 (R593Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287423	NM_003408.3(ZFP37):c.1886A>C (p.His629Pro)	ZFP37 (H630P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270125	NM_003408.3(ZFP37):c.421G>A (p.Val141Ile)	ZFP37 (V141I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267744	NM_003408.3(ZFP37):c.1797A>C (p.Lys599Asn)	ZFP37 (K600N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261837	NM_003408.3(ZFP37):c.1033G>A (p.Gly345Arg)	ZFP37 (G346R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220553	NM_003408.3(ZFP37):c.217T>C (p.Cys73Arg)	ZFP37 (C88R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206314	NM_003408.3(ZFP37):c.672G>T (p.Lys224Asn)	ZFP37 (K224N +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1707440	GRCh37/hg19 9q31.3-32(chr9:113673200-115935268)x1	DNAJC25, DNAJC25-GNG10 +19 more	Copy number loss	See cases	GUncertain significance
Select item 1703688	GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311)	ATOSB, ATP6V1G1 +417 more	Copy number loss	Distal tetrasomy 15q	GUncertain significance
Select item 1527542	GRCh37/hg19 9q31.2-32(chr9:109265628-117650999)	ABITRAM, ACTL7A +61 more	Copy number loss	not specified	GLikely pathogenic
Select item 1527539	GRCh37/hg19 9q31.1-33.3(chr9:104604851-126253089)	ABCA1, ABITRAM +130 more	Copy number loss	not specified	GPathogenic
Select item 1527521	GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410)	ABCA1, ABHD17B +261 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	AMBP, ANAPC2 +552 more	Copy number gain	not provided	GPathogenic
Select item 686835	GRCh37/hg19 9q31.3-32(chr9:113982711-117443628)x1	AKNA, ALAD +39 more	Copy number loss	not provided	GUncertain significance
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 563576	GRCh37/hg19 9q32(chr9:115801417-115881587)x1	ZFP37	Copy number loss	not provided	GUncertain significance
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ANGPTL2, ANKS6 +555 more	Copy number gain	Seizure +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	ODF2, OGN +769 more	Copy number gain	See cases	GPathogenic
Select item 442115	GRCh37/hg19 9q31.3-33.2(chr9:114299780-123267736)x1	AKNA, ALAD +48 more	Copy number loss	See cases	GPathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 395531	GRCh37/hg19 9q32(chr9:115761147-115818891)x1	ZFP37, ZNF883	Copy number loss	See cases	GLikely benign
Select item 394605	GRCh37/hg19 9q31.3-33.1(chr9:111348809-118687200)x1	ABITRAM, ACTL7A +61 more	Copy number loss	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 161058	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	LOC126860732, LOC126860733 +514 more	Copy number loss	See cases	GPathogenic
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 152171	GRCh38/hg38 9q31.2-33.1(chr9:107530314-117965944)x1	PALM2AKAP2, PAPPA +377 more	Copy number loss	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 91951	NM_003408.3(ZFP37):c.19G>C (p.Val7Leu)	LOC130002408, ZFP37 (V7L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 59881	GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3	LOC130002218, LOC130002219 +994 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59123	GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1	CT70, CTNNAL1 +509 more	Copy number loss	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 32222	GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1	ABCA1, ABITRAM +514 more	Copy number loss	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 70