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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2641926copy number variation1estd197human NCBI36 chr12: 6,821,195-6,821,195 , GRCh37.p13 chr12: 6,950,934-6,950,934 , GRCh37.p13 chr12|NW_003871083.2: 43,354-43,354 , GRCh38.p12 chr12: 6,841,770-6,841,770 GNB3
    esv2110276copy number variation1estd194human NCBI36 chr12: 6,821,192-6,821,193 , GRCh37.p13 chr12: 6,950,931-6,950,932 , GRCh37.p13 chr12|NW_003871083.2: 43,351-43,352 , GRCh38.p12 chr12: 6,841,767-6,841,768 GNB3
    esv2554393insertion1estd197human NCBI36 chr12: 6,820,511-6,820,511 , GRCh37.p13 chr12|NW_003871083.2: 42,670-42,670 , GRCh37.p13 chr12: 6,950,250-6,950,250 , GRCh38.p12 chr12: 6,841,086-6,841,086 GNB3
    esv2332276insertion1estd194human NCBI36 chr12: 6,820,512-6,820,512 , GRCh37.p13 chr12: 6,950,251-6,950,251 , GRCh37.p13 chr12|NW_003871083.2: 42,671-42,671 , GRCh38.p12 chr12: 6,841,087-6,841,087 GNB3
    nsv44561insertion1nstd6human NCBI35 chr12: 6,820,512-6,820,512 , GRCh37.p13 chr12|NW_003871083.2: 42,671-42,671 , GRCh37.p13 chr12: 6,950,251-6,950,251 , GRCh38.p12 chr12: 6,841,087-6,841,087 GNB3
    nsv1684526short tandem repeat3nstd128human GRCh37 chr12: 6,950,058-6,950,078 , GRCh38.p12 chr12: 6,840,894-6,840,914 GNB3
    nsv4198844copy number variation1nstd166human GRCh37.p13 chr12: 6,954,076-6,954,161 , GRCh38.p12 chr12: 6,844,912-6,844,997 GNB3, CDCA3
    nsv4195334copy number variation1nstd166human GRCh37.p13 chr12: 6,953,920-6,954,000 , GRCh38.p12 chr12: 6,844,756-6,844,836 GNB3, CDCA3
    nsv3158243copy number variation3nstd151human GRCh37 chr12: 6,952,335-6,952,406 , GRCh38.p12 chr12: 6,843,171-6,843,242 GNB3, CDCA3
    nsv516726copy number variation13nstd21human NCBI35 chr12: 6,818,289-6,819,143 , GRCh37.p13 chr12|NW_003871083.2: 40,448-41,302 , GRCh37.p13 chr12: 6,948,028-6,948,882 , GRCh38.p12 chr12: 6,838,864-6,839,718 GNB3, P3H3
    nsv526312copy number variation1nstd21human NCBI35 chr12: 6,818,729-6,819,160 , GRCh37.p13 chr12|NW_003871083.2: 40,888-41,319 , GRCh37.p13 chr12: 6,948,468-6,948,899 , GRCh38.p12 chr12: 6,839,304-6,839,735 GNB3, P3H3
    esv2899293insertion1estd209human GRCh37 chr12: 6,955,865-6,955,865 , GRCh38.p12 chr12: 6,846,701-6,846,701 GNB3, CDCA3
    nsv1650140short tandem repeat4nstd128human GRCh37 chr12: 6,955,840-6,955,884 , GRCh38.p12 chr12: 6,846,676-6,846,720 GNB3, CDCA3
    nsv1684531short tandem repeat1nstd128human GRCh37 chr12: 6,955,786-6,955,813 , GRCh38.p12 chr12: 6,846,622-6,846,649 GNB3, CDCA3
    nsv1650123short tandem repeat1nstd128human GRCh37 chr12: 6,948,500-6,948,525 , GRCh38.p12 chr12: 6,839,336-6,839,361 GNB3, P3H3
    nsv1684530short tandem repeat1nstd128human GRCh37 chr12: 6,953,939-6,953,956 , GRCh38.p12 chr12: 6,844,775-6,844,792 GNB3, CDCA3
    nsv6309486copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,950,452-6,979,547 , GRCh38.p12 chr12: 6,841,288-6,870,383 GNB3, TPI1, 3 more genes
    nsv898638copy number variation1nstd71human NCBI36 chr12: 6,799,898-6,825,125 , GRCh37.p13 chr12|NW_003871083.2: 22,057-47,284 , GRCh37.p13 chr12: 6,929,637-6,954,864 , GRCh38.p12 chr12: 6,820,471-6,845,700 GNB3, P3H3, 3 more genes
    nsv3913712copy number variation1nstd102humanPathogenic NCBI36 chr12: 6,708,092-7,749,483 , GRCh37 chr12: 6,837,831-7,858,216 , GRCh38 chr12: 6,728,665-7,705,620 GNB3, MIR141, 49 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 GNB3, RNA5SP369, 2454 more genes
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