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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6897918copy number variation1nstd229human GRCh38 chr10: 114,285,399-114,292,178 , GRCh37.p13 chr10: 116,045,158-116,051,937 VWA2, AFAP1L2
    nsv6897527copy number variation1nstd229human GRCh38 chr10: 114,262,834-114,272,144 , GRCh37.p13 chr10: 116,022,593-116,031,903 VWA2
    nsv6896883copy number variation1nstd229human GRCh38 chr10: 114,264,698-114,267,722 , GRCh37.p13 chr10: 116,024,457-116,027,481 VWA2
    nsv6896709copy number variation1nstd229human GRCh38 chr10: 114,287,868-114,287,896 , GRCh37.p13 chr10: 116,047,627-116,047,655 VWA2, AFAP1L2
    nsv6895103copy number variation1nstd229human GRCh38 chr10: 114,249,948-114,252,432 , GRCh37.p13 chr10: 116,009,707-116,012,191 VWA2
    nsv6892118copy number variation1nstd229human GRCh38 chr10: 114,249,042-114,255,990 , GRCh37.p13 chr10: 116,008,801-116,015,749 VWA2
    nsv6889017copy number variation1nstd229human GRCh38 chr10: 114,270,582-115,684,161 , GRCh37.p13 chr10: 116,030,341-116,786,295 RN7SL384P, ATRNL1, 14 more genes
    nsv6887181copy number variation1nstd229human GRCh38 chr10: 114,281,201-114,284,600 , GRCh37.p13 chr10: 116,040,960-116,044,359 AFAP1L2, VWA2
    nsv6886446copy number variation1nstd229human GRCh38 chr10: 114,269,315-114,274,211 , GRCh37.p13 chr10: 116,029,074-116,033,970 VWA2
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6879715copy number variation1nstd229human GRCh38 chr10: 114,255,956-114,262,873 , GRCh37.p13 chr10: 116,015,715-116,022,632 VWA2
    nsv6589006inversion1nstd223human GRCh38 chr10: 114,253,715-114,255,334 , GRCh37.p13 chr10: 116,013,474-116,015,093 VWA2
    nsv6452921copy number variation1nstd223human GRCh38 chr10: 114,263,516-114,267,559 , GRCh37.p13 chr10: 116,023,275-116,027,318 VWA2
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6137347translocation1nstd213human GRCh38.p12 chr14: 61,397,119-61,397,119 , GRCh37 chr14: 61,863,837-61,863,837 , GRCh38.p12 chr10: 114,252,733-114,252,733 , GRCh37 chr10: 116,012,492-116,012,492 PRKCH, VWA2
    nsv6132019copy number variation1nstd213human GRCh37 chr10: 115,120,000-116,220,001 , GRCh38.p12 chr10: 113,360,241-114,460,242 CASP7, MIR2110, 21 more genes
    nsv6131932copy number variation1nstd213human GRCh37 chr10: 115,960,000-125,870,001 , GRCh38.p12 chr10: 114,200,241-124,109,956 ACADSB, DMBT1, 148 more genes
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