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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093839copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,757,550-17,758,139 , GRCh38.p12 chr11: 17,736,003-17,736,592 KCNC1
    nsv7076169inversion1nstd229human GRCh38 chr11: 17,779,353-17,780,799 , GRCh37.p13 chr11: 17,800,900-17,802,346 KCNC1
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv7067983inversion1nstd229human GRCh38 chr11: 17,304,327-18,032,820 , GRCh37.p13 chr11: 17,325,874-18,054,367 LOC107984317, LINC02729, 12 more genes
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6916591copy number variation1nstd229human GRCh38 chr11: 17,708,484-17,750,483 , GRCh37.p13 chr11: 17,730,031-17,772,030 MYOD1, KCNC1
    nsv6911337copy number variation1nstd229human GRCh38 chr11: 17,746,640-17,748,581 , GRCh37.p13 chr11: 17,768,187-17,770,128 KCNC1
    nsv6909685copy number variation1nstd229human GRCh38 chr11: 17,770,462-17,770,642 , GRCh37.p13 chr11: 17,792,009-17,792,189 KCNC1
    nsv6905748copy number variation1nstd229human GRCh38 chr11: 17,779,424-17,779,585 , GRCh37.p13 chr11: 17,800,971-17,801,132 KCNC1
    nsv6902492copy number variation1nstd229human GRCh38 chr11: 17,764,263-17,764,302 , GRCh37.p13 chr11: 17,785,810-17,785,849 KCNC1
    nsv6902066copy number variation1nstd229human GRCh38 chr11: 17,747,266-17,757,193 , GRCh37.p13 chr11: 17,768,813-17,778,740 KCNC1
    nsv6637654copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,784,556-18,797,650 , GRCh38.p12 chr11: 17,763,009-18,776,103 LOC112268073, SAAL1, 37 more genes
    nsv6620970copy number variation1nstd224human GRCh37 chr11: 17,757,417-18,073,039 , GRCh38.p12 chr11: 17,735,870-18,051,492 KCNC1, LOC107984317, 2 more genes
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 more genes
    nsv6441415copy number variation1nstd223human GRCh38 chr11: 17,708,484-17,750,480 , GRCh37.p13 chr11: 17,730,031-17,772,027 KCNC1, MYOD1
    nsv6437652copy number variation1nstd223human GRCh38 chr11: 17,779,366-17,780,677 , GRCh37.p13 chr11: 17,800,913-17,802,224 KCNC1
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6303966copy number variation1nstd186human GRCh37 chr11: 17,754,480-17,755,810 , GRCh38.p12 chr11: 17,732,933-17,734,263 KCNC1
    nsv6274867copy number variation1nstd214human GRCh38 chr11: 17,763,579-17,763,791 , GRCh37.p13 chr11: 17,785,126-17,785,338 KCNC1
    nsv6271830copy number variation1nstd214human GRCh38 chr11: 17,763,575-17,763,791 , GRCh37.p13 chr11: 17,785,122-17,785,338 KCNC1
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