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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977049insertion1nstd209human GRCh38 chr17: 29,083,512-29,083,512 , GRCh37.p13 chr17: 27,410,530-27,410,530 MYO18A
    nsv5943117copy number variation1nstd209human GRCh38 chr17: 29,168,438-29,168,494 , GRCh37.p13 chr17: 27,495,456-27,495,512 MYO18A
    nsv5938302copy number variation1nstd209human GRCh38 chr17: 29,105,796-29,106,053 , GRCh37.p13 chr17: 27,432,814-27,433,071 MYO18A
    nsv5929769copy number variation1nstd209human GRCh38 chr17: 29,087,736-29,088,345 , GRCh37.p13 chr17: 27,414,754-27,415,363 MYO18A
    nsv5929003copy number variation1nstd209human GRCh38 chr17: 29,125,915-29,127,820 , GRCh37.p13 chr17: 27,452,933-27,454,838 MYO18A
    nsv5877047copy number variation1nstd209human GRCh38 chr17: 29,125,934-29,127,878 , GRCh37.p13 chr17: 27,452,952-27,454,896 MYO18A
    nsv5532350copy number variation1nstd206human GRCh38 chr17: 29,138,218-29,138,794 , GRCh37.p13 chr17: 27,465,236-27,465,812 MYO18A
    nsv5531281copy number variation1nstd206human GRCh38 chr17: 29,081,452-29,081,524 , GRCh37.p13 chr17: 27,408,470-27,408,542 MYO18A
    nsv5530071copy number variation1nstd206human GRCh38 chr17: 29,105,796-29,106,061 , GRCh37.p13 chr17: 27,432,814-27,433,079 MYO18A
    nsv5526250copy number variation1nstd206human GRCh38 chr17: 29,168,440-29,168,495 , GRCh37.p13 chr17: 27,495,458-27,495,513 MYO18A
    nsv5523121copy number variation1nstd206human GRCh38 chr17: 29,087,743-29,088,346 , GRCh37.p13 chr17: 27,414,761-27,415,364 MYO18A
    nsv5521362copy number variation1nstd206human GRCh38 chr17: 29,137,848-29,143,855 , GRCh37.p13 chr17: 27,464,866-27,470,873 MYO18A
    nsv5520530copy number variation1nstd206human GRCh38 chr17: 29,124,493-29,124,570 , GRCh37.p13 chr17: 27,451,511-27,451,588 MYO18A
    nsv5519304copy number variation1nstd206human GRCh38 chr17: 29,078,606-29,079,340 , GRCh37.p13 chr17: 27,405,624-27,406,358 MYO18A
    nsv5374872translocation1nstd200human GRCh38 chr17: 29,127,541-29,127,541 , GRCh38 chr17: 44,281,059-44,281,059 , GRCh37.p13 chr17: 42,358,427-42,358,427 , GRCh37.p13 chr17: 27,454,559-27,454,559 MYO18A
    nsv5358780translocation1nstd200human GRCh38 chr17: 29,106,061-29,106,061 , GRCh38 chr17: 29,105,796-29,105,796 , GRCh37.p13 chr17: 27,432,814-27,432,814 , GRCh37.p13 chr17: 27,433,079-27,433,079 MYO18A
    nsv5358779translocation1nstd200human GRCh38 chr17: 29,088,346-29,088,346 , GRCh38 chr17: 29,087,743-29,087,743 , GRCh37.p13 chr17: 27,414,761-27,414,761 , GRCh37.p13 chr17: 27,415,364-27,415,364 MYO18A
    nsv5340143translocation1nstd200human GRCh37 chr17: 42,358,427-42,358,427 , GRCh37 chr17: 27,454,559-27,454,559 , GRCh38.p12 chr17: 44,281,059-44,281,059 , GRCh38.p12 chr17: 29,127,541-29,127,541 MYO18A
    nsv5337771translocation1nstd200human GRCh37 chr17: 27,414,761-27,414,761 , GRCh37 chr17: 27,415,364-27,415,364 , GRCh38.p12 chr17: 29,087,743-29,087,743 , GRCh38.p12 chr17: 29,088,346-29,088,346 MYO18A
    nsv5326975copy number variation1nstd204human GRCh38.p13 chr17: 29,143,731-29,144,162 , GRCh37.p13 chr17: 27,470,749-27,471,180 MYO18A
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