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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971071inversion1nstd209human GRCh38 chr13: 110,954,328-112,396,498 , GRCh37.p13 chr13: 111,606,675-112,978,183 SOX1, ARHGEF7, 28 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4834301copy number variation1nstd200human GRCh37 chr13: 112,814,548-112,851,562 , GRCh38.p12 chr13: 112,160,234-112,182,875 LOC105370370, LOC100506016
    nsv4769247copy number variation1nstd201human GRCh37 chr13: 109,490,236-115,107,733 , GRCh38.p12 chr13: 108,837,888-114,342,258 , PARP1P1, 117 more genes
    nsv4729336copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 112,069,981-115,107,733 , GRCh38.p12 chr13: 111,417,634-114,342,258 ATP4B, F7, 68 more genes
    nsv4728884copy number variation1nstd102humanPathogenic GRCh37 chr13: 106,256,198-115,107,733 , GRCh38.p12 chr13: 105,603,849-114,342,258 LINC01044, CARS2, 139 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
    nsv4504630mobile element insertion1nstd166human GRCh37.p13 chr13: 112,810,381-112,810,381 , GRCh38.p12 chr13: 112,156,067-112,156,067 LOC100506016
    nsv4457030copy number variation1nstd102humanPathogenic GRCh37 chr13: 111,568,865-115,107,733 , GRCh38.p12 chr13: 110,916,518-114,342,258 ARHGEF7, LINC00431, 79 more genes
    nsv4456643copy number variation1nstd102humanUncertain significance GRCh37 chr13: 112,352,288-112,990,608 , GRCh38.p12 chr13: 111,699,941-112,323,869 LOC101928730, LOC107984555, 10 more genes
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4456505copy number variation1nstd102humanUncertain significance GRCh37 chr13: 109,203,109-115,107,733 , GRCh38.p12 chr13: 108,550,761-114,342,258 LINC01054, GAS6-DT, 111 more genes
    nsv4456260copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,849,303-115,107,733 , GRCh38.p12 chr13: 94,197,049-114,342,258 F10, FKSG29, 300 more genes
    nsv4452838copy number variation1nstd102humannot provided GRCh37 chr13: 107,452,288-115,092,569 , GRCh38.p12 chr13: 106,799,940-114,327,094 LOC105370360, COL4A1, 122 more genes
    nsv4381212copy number variation1nstd173human GRCh37 chr13: 112,613,712-115,107,745 , GRCh38.p12 chr13: 111,959,398-114,342,270 , LOC105370372, 66 more genes
    nsv4348837copy number variation1nstd102humanPathogenic GRCh37 chr13: 101,881,803-115,091,330 , GRCh38.p12 chr13: 101,229,452-114,325,855 RN7SL783P, EFNB2, 181 more genes
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