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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936890copy number variation1nstd209human GRCh38 chr12: 110,383,797-110,384,124 , GRCh37.p13 chr12: 110,821,602-110,821,929 ANAPC7
    nsv5855791copy number variation1nstd209human GRCh38 chr12: 110,378,427-110,379,826 , GRCh37.p13 chr12: 110,816,232-110,817,631 ANAPC7
    nsv5664329insertion1nstd207human GRCh38 chr12: 110,387,383-110,387,383 , GRCh37.p13 chr12: 110,825,188-110,825,188 ANAPC7
    nsv5273674copy number variation1nstd204human GRCh37.p13 chr12: 110,813,506-110,955,705 , GRCh38.p13 chr12: 110,375,701-110,517,900 ARPC3, FAM216A, 6 more genes
    nsv4995576copy number variation1nstd200human GRCh38 chr12: 110,401,882-110,402,047 , GRCh37.p13 chr12: 110,839,687-110,839,852 ANAPC7
    nsv4995575copy number variation1nstd200human GRCh38 chr12: 110,389,665-110,390,792 , GRCh37.p13 chr12: 110,827,470-110,828,597 ANAPC7
    nsv4995574copy number variation1nstd200human GRCh38 chr12: 110,371,912-110,372,416 , GRCh37.p13 chr12: 110,809,717-110,810,221 ANAPC7
    nsv4993673copy number variation1nstd200human GRCh38 chr12: 110,368,992-110,446,801 , GRCh37.p13 chr12: 110,806,797-110,884,606 HMGA1P3, ARPC3, 1 more genes
    nsv4842695copy number variation1nstd200human GRCh37 chr12: 110,839,687-110,839,852 , GRCh38.p12 chr12: 110,401,882-110,402,047 ANAPC7
    nsv4833066copy number variation1nstd200human GRCh37 chr12: 110,827,470-110,828,597 , GRCh38.p12 chr12: 110,389,665-110,390,792 ANAPC7
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 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
    nsv4730349copy number variation1nstd199human GRCh37 chr12: 110,825,042-110,825,107 , GRCh38.p12 chr12: 110,387,237-110,387,302 ANAPC7
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 ATP2A2, CUX2, 115 more genes
    nsv4500148mobile element insertion1nstd166human GRCh37.p13 chr12: 110,838,310-110,838,310 , GRCh38.p12 chr12: 110,400,505-110,400,505 ANAPC7
    nsv4228781copy number variation1nstd166human GRCh37.p13 chr12: 110,807,551-110,810,585 , GRCh38.p12 chr12: 110,369,746-110,372,780 ANAPC7
    nsv4220253copy number variation1nstd166human GRCh37.p13 chr12: 110,810,852-110,810,962 , GRCh38.p12 chr12: 110,373,047-110,373,157 ANAPC7
    nsv4218504copy number variation1nstd166human GRCh37.p13 chr12: 110,839,688-110,839,851 , GRCh38.p12 chr12: 110,401,883-110,402,046 ANAPC7
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