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Items: 1 to 20 of 68

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6917497copy number variation1nstd229human GRCh38 chr11: 17,834,501-17,899,700 , GRCh37.p13 chr11: 17,856,048-17,921,247 LOC107984317, SERGEF
    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
    nsv6914521copy number variation1nstd229human GRCh38 chr11: 17,840,657-17,884,995 , GRCh37.p13 chr11: 17,862,204-17,906,542 SERGEF, LOC107984317
    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
    nsv6448731copy number variation1nstd223human GRCh38 chr11: 17,854,217-17,858,136 , GRCh37.p13 chr11: 17,875,764-17,879,683 LOC107984317, SERGEF
    nsv6435735copy number variation1nstd223human GRCh38 chr11: 17,840,657-17,884,994 , GRCh37.p13 chr11: 17,862,204-17,906,541 LOC107984317, SERGEF
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv4978438copy number variation1nstd200human GRCh38 chr11: 17,840,657-17,884,994 , GRCh37.p13 chr11: 17,862,204-17,906,541 SERGEF, LOC107984317
    nsv4834340copy number variation1nstd200human GRCh37 chr11: 17,862,204-17,906,541 , GRCh38.p12 chr11: 17,840,657-17,884,994 LOC107984317, SERGEF
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4675008copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,873,318-17,952,629 , GRCh38.p12 chr11: 17,851,771-17,931,082 SERGEF, LOC107984317
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