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Items: 1 to 20 of 982

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118101copy number variation1nstd186human GRCh37 chr2: 153,205,336-153,205,649 , GRCh38.p12 chr2: 152,348,822-152,349,135 FMNL2
    nsv5980342inversion1nstd209human GRCh38 chr2: 152,603,401-152,604,920 , GRCh37.p13 chr2: 153,459,915-153,461,434 FMNL2
    nsv5974630inversion1nstd209human GRCh38 chr2: 152,604,934-152,605,286 , GRCh37.p13 chr2: 153,461,448-153,461,800 FMNL2
    nsv5957403insertion1nstd209human GRCh38 chr2: 152,391,751-152,391,751 , GRCh37.p13 chr2: 153,248,265-153,248,265 FMNL2
    nsv5906665copy number variation1nstd209human GRCh38 chr2: 152,646,574-152,646,638 , GRCh37.p13 chr2: 153,503,088-153,503,152 , FMNL2
    nsv5901424copy number variation1nstd209human GRCh38 chr2: 152,489,150-152,489,246 , GRCh37.p13 chr2: 153,345,664-153,345,760 FMNL2
    nsv5895904copy number variation1nstd209human GRCh38 chr2: 152,542,611-152,542,663 , GRCh37.p13 chr2: 153,399,125-153,399,177 FMNL2
    nsv5892810copy number variation1nstd209human GRCh38 chr2: 152,324,770-152,713,685 , GRCh37.p13 chr2: 153,181,284-153,570,199 , NUDCP1, 2 more genes
    nsv5892645copy number variation1nstd209human GRCh38 chr2: 152,421,174-152,421,276 , GRCh37.p13 chr2: 153,277,688-153,277,790 FMNL2
    nsv5890808copy number variation1nstd209human GRCh38 chr2: 152,612,764-152,612,834 , GRCh37.p13 chr2: 153,469,278-153,469,348 FMNL2
    nsv5831869copy number variation1nstd209human GRCh38 chr2: 152,543,117-152,544,536 , GRCh37.p13 chr2: 153,399,631-153,401,050 FMNL2
    nsv5831868copy number variation2nstd209human GRCh38 chr2: 152,451,328-152,452,839 , GRCh37.p13 chr2: 153,307,842-153,309,353 FMNL2
    nsv5831867copy number variation1nstd209human GRCh38 chr2: 152,413,392-152,414,591 , GRCh37.p13 chr2: 153,269,906-153,271,105 FMNL2
    nsv5831661copy number variation1nstd209human GRCh38 chr2: 152,508,771-152,631,423 , GRCh37.p13 chr2: 153,365,285-153,487,937 FMNL2
    nsv5831660copy number variation2nstd209human GRCh38 chr2: 152,466,790-152,467,889 , GRCh37.p13 chr2: 153,323,304-153,324,403 FMNL2
    nsv5831658copy number variation2nstd209human GRCh38 chr2: 152,338,570-152,341,247 , GRCh37.p13 chr2: 153,195,084-153,197,761 FMNL2
    nsv5831645copy number variation2nstd209human GRCh38 chr2: 152,627,087-152,628,086 , GRCh37.p13 chr2: 153,483,601-153,484,600 FMNL2
    nsv5831644copy number variation1nstd209human GRCh38 chr2: 152,603,439-152,604,538 , GRCh37.p13 chr2: 153,459,953-153,461,052 FMNL2
    nsv5831643copy number variation1nstd209human GRCh38 chr2: 152,603,322-152,604,538 , GRCh37.p13 chr2: 153,459,836-153,461,052 FMNL2
    nsv5831641copy number variation1nstd209human GRCh38 chr2: 152,324,674-152,354,304 , GRCh37.p13 chr2: 153,181,188-153,210,818 FMNL2
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