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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5509709copy number variation1nstd206human GRCh38 chr12: 92,116,508-92,143,103 , GRCh37.p13 chr12: 92,510,284-92,536,879 LINC01619, BTG1
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4993553copy number variation1nstd200human GRCh38 chr12: 92,116,508-92,143,103 , GRCh37.p13 chr12: 92,510,284-92,536,879 BTG1, LINC01619
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4843573copy number variation1nstd200human GRCh37 chr12: 92,510,284-92,536,879 , GRCh38.p12 chr12: 92,116,508-92,143,103 LINC01619, BTG1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4616088copy number variation1nstd183human GRCh37 chr12: 92,534,025-92,539,619 , GRCh38.p12 chr12: 92,140,249-92,145,843 , LINC01619, 2 more genes
    nsv4601415copy number variation1nstd183human GRCh37 chr12: 92,512,011-92,540,212 , GRCh38.p12 chr12: 92,118,235-92,146,436 , LINC01619, 2 more genes
    nsv4456763copy number variation1nstd102humanPathogenic GRCh37 chr12: 77,737,623-94,330,526 , GRCh38.p12 chr12: 77,343,843-93,936,750 MIR1252, PLEKHG7, 162 more genes
    nsv4431850copy number variation1nstd172human GRCh38.p12 chr12: 92,128,225-92,147,224 , GRCh37.p13 chr12: 92,522,001-92,541,000 , BTG1, 2 more genes
    nsv4417588copy number variation1nstd174human GRCh37 chr12: 92,506,140-92,539,620 , GRCh38.p12 chr12: 92,112,364-92,145,844 , BTG1, 2 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4325802inversion1nstd166human GRCh37.p13 chr12: 70,180,810-110,320,028 , GRCh38.p12 chr12: 69,787,030-109,882,223 , APAF1, 540 more genes
    nsv4229807copy number variation1nstd166human GRCh37.p13 chr12: 92,510,284-92,536,891 , GRCh38.p12 chr12: 92,116,508-92,143,115 LINC01619, BTG1
    nsv4218001copy number variation1nstd166human GRCh37.p13 chr12: 92,537,000-92,542,100 , GRCh38.p12 chr12: 92,143,224-92,148,324 , LINC01619, 2 more genes
    nsv3960041copy number variation1nstd168human GRCh38 chr12: 92,007,078-92,171,712 , GRCh37.p13 chr12: 92,400,854-92,565,488 , BTG1, 3 more genes
    nsv3924338copy number variation1nstd102humanPathogenic NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015 NUP37, TTC41P, 295 more genes
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