ClinVar for Gene (Select 55321) - ClinVar

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Links from Gene

Items: 71

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3327179	NM_001304748.2(TMEM74B):c.500C>T (p.Ala167Val)	TMEM74B (A143V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179644	NM_001304748.2(TMEM74B):c.88G>C (p.Gly30Arg)	TMEM74B (G30R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179643	NM_001304748.2(TMEM74B):c.619C>T (p.Arg207Trp)	TMEM74B (R207W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179641	NM_001304748.2(TMEM74B):c.29C>T (p.Ala10Val)	TMEM74B (A10V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179640	NM_001304748.2(TMEM74B):c.298G>A (p.Asp100Asn)	TMEM74B (D100N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3179639	NM_001304748.2(TMEM74B):c.296G>A (p.Arg99Gln)	TMEM74B (R75Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3024619	GRCh37/hg19 20p13-11.21(chr20:68351-23860313)x3	RAD21L1, RALGAPA2 +164 more	Copy number gain	not provided	GPathogenic
Select item 3024618	GRCh37/hg19 20p13-12.1(chr20:68351-16142323)x3	SIRPB2, SIRPD +114 more	Copy number gain	not provided	GPathogenic
Select item 2684899	GRCh37/hg19 20p13-12.2(chr20:61569-9542361)x3	ADAM33, ADISSP +100 more	Copy number gain	not provided	GPathogenic
Select item 2684898	GRCh37/hg19 20p13(chr20:61569-1794919)x3	ANGPT4, C20orf202 +31 more	Copy number gain	not provided	GUncertain significance
Select item 2671592	Single allele	C20orf202, ZCCHC3 +35 more	Deletion	not provided	GPathogenic
Select item 2579201	GRCh38/hg38 20p13-11.21(chr20:87153-23635465)x3	ADAM33, ADISSP +731 more	Copy number gain	Renal agenesis	GPathogenic
Select item 2559470	NM_001304748.2(TMEM74B):c.89G>C (p.Gly30Ala)	TMEM74B (G30A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536921	NM_001304748.2(TMEM74B):c.52G>A (p.Glu18Lys)	TMEM74B (E18K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522755	NM_001304748.2(TMEM74B):c.205C>T (p.His69Tyr)	TMEM74B (H45Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514717	NM_001304748.2(TMEM74B):c.617G>A (p.Arg206His)	TMEM74B (R182H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514098	NM_001304748.2(TMEM74B):c.631G>A (p.Val211Ile)	TMEM74B (V187I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399747	NM_001304748.2(TMEM74B):c.607G>A (p.Glu203Lys)	TMEM74B (E179K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399223	NM_001304748.2(TMEM74B):c.470G>A (p.Arg157Gln)	TMEM74B (R133Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397130	NM_001304748.2(TMEM74B):c.382G>A (p.Val128Ile)	TMEM74B (V104I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381987	NM_001304748.2(TMEM74B):c.554C>T (p.Thr185Met)	TMEM74B (T161M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369004	NM_001304748.2(TMEM74B):c.350G>A (p.Arg117His)	TMEM74B (R93H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314077	NM_001304748.2(TMEM74B):c.709G>T (p.Ala237Ser)	TMEM74B (A213S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280557	NM_001304748.2(TMEM74B):c.225C>G (p.Asn75Lys)	TMEM74B (N51K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235287	NM_001304748.2(TMEM74B):c.356T>C (p.Val119Ala)	TMEM74B (V95A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1809250	GRCh37/hg19 20p13(chr20:992980-1481478)x4	C20orf202, FKBP1A +7 more	Copy number gain	not provided	GUncertain significance
Select item 1808289	GRCh37/hg19 20p13(chr20:1015167-1403720)x3	C20orf202, FKBP1A +5 more	Copy number gain	not provided	GUncertain significance
Select item 1526676	GRCh37/hg19 20p13(chr20:61568-1823540)	ANGPT4, C20orf202 +31 more	Copy number loss	not specified	GPathogenic
Select item 816104	GRCh37/hg19 20p13(chr20:989820-1216980)x3	C20orf202, RAD21L1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 816102	GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3	ABHD12, ACSS1 +177 more	Copy number gain	not provided	GPathogenic
Select item 816101	GRCh37/hg19 20p13(chr20:61568-1305971)x1	ANGPT4, C20orf202 +25 more	Copy number loss	not provided	GPathogenic
Select item 816099	GRCh37/hg19 20p13(chr20:61568-2269777)x1	DEFB132, FAM110A +34 more	Copy number loss	not provided	GPathogenic
Select item 688959	GRCh37/hg19 20p13(chr20:728577-1237670)x4	ANGPT4, C20orf202 +6 more	Copy number gain	not provided	GUncertain significance
Select item 564643	GRCh37/hg19 20p13(chr20:61568-2010334)x1	ANGPT4, C20orf202 +33 more	Copy number loss	not provided	GLikely pathogenic
Select item 443774	GRCh37/hg19 20p13-12.2(chr20:61568-10486106)x3	ADAM33, ADISSP +104 more	Copy number gain	See cases	GLikely pathogenic
Select item 443574	GRCh37/hg19 20p13(chr20:381794-1268103)x3	ANGPT4, C20orf202 +13 more	Copy number gain	See cases	GUncertain significance
Select item 443340	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 443339	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 443248	GRCh37/hg19 20p13-12.3(chr20:213423-5483406)x3	ADAM33, ADISSP +80 more	Copy number gain	See cases	GUncertain significance
Select item 442743	GRCh37/hg19 20p13(chr20:61568-2824960)x3	NSFL1C, PCED1A +48 more	Copy number gain	See cases	GUncertain significance
Select item 441596	GRCh37/hg19 20p13(chr20:61568-1651420)x1	ANGPT4, C20orf202 +31 more	Copy number loss	See cases	GLikely pathogenic
Select item 424642	GRCh37/hg19 20p13-q11.21(chr20:80198-26208081)x3	ESF1, FAM110A +178 more	Copy number gain	not provided	GPathogenic
Select item 394598	GRCh37/hg19 20p13(chr20:1164613-1229292)x3	C20orf202, RAD21L1 +1 more	Copy number gain	See cases	GUncertain significance
Select item 393750	GRCh37/hg19 20p13(chr20:121521-2073612)x1	ANGPT4, C20orf202 +32 more	Copy number loss	See cases	GPathogenic
Select item 253647	GRCh37/hg19 20p13-11.1(chr20:80198-26075841)x3	ABHD12, ACSS1 +176 more	Copy number gain	See cases	GPathogenic
Select item 253566	GRCh37/hg19 20p13-12.3(chr20:121521-5564937)x3	ADAM33, ADISSP +85 more	Copy number gain	See cases	GPathogenic
Select item 202236	GRCh37/hg19 20p13(chr20:71023-2129746)x1	NRSN2, SIRPD +34 more	Copy number loss	See cases	GPathogenic
Select item 161074	GRCh38/hg38 20p13(chr20:89939-1852477)x1	ANGPT4, C20orf202 +104 more	Copy number loss	See cases	GPathogenic
Select item 155633	GRCh38/hg38 20p13(chr20:80927-1806080)x1	ANGPT4, C20orf202 +103 more	Copy number loss	See cases	GLikely pathogenic
Select item 155359	GRCh38/hg38 20p13-11.23(chr20:80928-18688031)x3	ADAM33, ADISSP +571 more	Copy number gain	See cases	GPathogenic
Select item 154852	GRCh38/hg38 20p13(chr20:80106-1246891)x1	ANGPT4, C20orf202 +76 more	Copy number loss	See cases	GLikely pathogenic
Select item 154176	GRCh38/hg38 20p13-12.3(chr20:80927-5447679)x3	LOC112694699, LOC112694712 +306 more	Copy number gain	See cases	GUncertain significance
Select item 153731	GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3	ABHD12, ACSS1 +828 more	Copy number gain	See cases	GPathogenic
Select item 152841	GRCh38/hg38 20p13-12.3(chr20:84402-6159078)x3	LOC114004355, LOC116286198 +347 more	Copy number gain	See cases	GPathogenic
Select item 152298	GRCh38/hg38 20p13(chr20:209424-1852477)x3	ANGPT4, C20orf202 +100 more	Copy number gain	See cases	GUncertain significance
Select item 150785	GRCh38/hg38 20p13-12.3(chr20:80093-6386012)x3	LOC130065401, LOC130065402 +348 more	Copy number gain	See cases	GPathogenic
Select item 150565	GRCh38/hg38 20p13(chr20:80093-1246766)x1	ANGPT4, C20orf202 +76 more	Copy number loss	See cases	GPathogenic
Select item 149704	GRCh38/hg38 20p13-12.1(chr20:80106-13029401)x3	LOC130065344, LOC130065345 +455 more	Copy number gain	See cases	GPathogenic
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	JPH2, KAT14 +2522 more	Copy number gain	See cases	GPathogenic
Select item 146529	GRCh38/hg38 20p13(chr20:89939-1494113)x1	DEFB129, DEFB132 +96 more	Copy number loss	See cases	GPathogenic
Select item 146515	GRCh38/hg38 20p13(chr20:89939-1246891)x3	ANGPT4, C20orf202 +76 more	Copy number gain	See cases	GUncertain significance
Select item 144514	GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3	LOC129456123, LOC130065248 +833 more	Copy number gain	See cases	GPathogenic
Select item 59191	GRCh38/hg38 20p13-11.23(chr20:89939-19071495)x3	ADAM33, ADISSP +579 more	Copy number gain	See cases	GPathogenic
Select item 58945	GRCh38/hg38 20p13(chr20:121781-2290194)x1	ANGPT4, C20orf202 +120 more	Copy number loss	See cases	GPathogenic
Select item 58943	GRCh38/hg38 20p13(chr20:89939-1770567)x1	ANGPT4, C20orf202 +102 more	Copy number loss	See cases	GPathogenic
Select item 58942	GRCh38/hg38 20p13(chr20:89939-1939218)x1	LOC129391148, LOC129391149 +110 more	Copy number loss	See cases	GPathogenic
Select item 58940	GRCh38/hg38 20p13(chr20:828964-1241192)x3	ANGPT4, C20orf202 +21 more	Copy number gain	See cases	GUncertain significance
Select item 57514	GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3	FASTKD5, FERMT1 +814 more	Copy number gain	See cases	GPathogenic
Select item 57354	GRCh38/hg38 20p13-11.23(chr20:89939-19146279)x3	LOC130065324, LOC130065325 +581 more	Copy number gain	See cases	GPathogenic
Select item 57188	GRCh38/hg38 20p13(chr20:89939-1360110)x1	ANGPT4, C20orf202 +87 more	Copy number loss	See cases	GPathogenic
Select item 35265	GRCh38/hg38 20p13(chr20:89939-1852477)x1	ANGPT4, C20orf202 +104 more	Copy number loss	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 71