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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957294insertion1nstd209human GRCh38 chr5: 180,797,843-180,797,843 , GRCh37.p13 chr5: 180,224,843-180,224,843 MGAT1
    nsv5642764insertion1nstd207human GRCh38 chr5: 180,783,997-180,783,997 , GRCh37.p13 chr5: 180,210,997-180,210,997 MGAT1
    nsv5635244insertion1nstd207human GRCh38 chr5: 180,788,634-180,788,634 , GRCh37.p13 chr5: 180,215,634-180,215,634 MGAT1
    nsv5634761insertion1nstd207human GRCh38 chr5: 180,797,843-180,797,843 , GRCh37.p13 chr5: 180,224,843-180,224,843 MGAT1
    nsv5633748insertion1nstd207human GRCh38 chr5: 180,795,941-180,795,941 , GRCh37.p13 chr5: 180,222,941-180,222,941 MGAT1
    nsv5583879copy number variation1nstd207human GRCh38 chr5: 180,788,634-180,788,691 , GRCh37.p13 chr5: 180,215,634-180,215,691 MGAT1
    nsv5542261insertion1nstd206human GRCh38 chr5: 180,797,844-180,797,894 , GRCh37.p13 chr5: 180,224,844-180,224,894 MGAT1
    nsv5463196copy number variation1nstd206human GRCh38 chr5: 180,684,834-180,791,724 , GRCh37.p13 chr5: 180,111,834-180,218,724 LINC02222, MGAT1, 3 more genes
    nsv5099012mobile element insertion1nstd203human GRCh38 chr5: 180,807,856-180,807,874 , GRCh37.p13 chr5: 180,234,856-180,234,874 MGAT1
    nsv5081880mobile element insertion1nstd203human GRCh38 chr5: 180,786,354-180,786,368 , GRCh37.p13 chr5: 180,213,354-180,213,368 MGAT1
    nsv5081543mobile element insertion1nstd203human GRCh38 chr5: 180,815,753-180,815,761 , GRCh37.p13 chr5: 180,242,753-180,242,761 , MGAT1
    nsv4949315copy number variation1nstd200human GRCh38 chr5: 180,684,834-180,791,724 , GRCh37.p13 chr5: 180,111,834-180,218,724 OR2AI1P, LINC02222, 3 more genes
    nsv4940223copy number variation1nstd200human GRCh38 chr5: 180,801,989-180,806,330 , GRCh37.p13 chr5: 180,228,989-180,233,330 MGAT1
    nsv4828426copy number variation1nstd200human GRCh37 chr5: 180,111,834-180,218,724 , GRCh38.p12 chr5: 180,684,834-180,791,724 OR2AI1P, LINC02222, 3 more genes
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4768114insertion1nstd199human GRCh37 chr5: 180,215,657-180,215,657 , GRCh38.p12 chr5: 180,788,657-180,788,657 MGAT1
    nsv4762722insertion1nstd199human GRCh37 chr5: 180,222,979-180,222,979 , GRCh38.p12 chr5: 180,795,979-180,795,979 MGAT1
    nsv4758556insertion1nstd199human GRCh37 chr5: 180,224,808-180,224,808 , GRCh38.p12 chr5: 180,797,808-180,797,808 MGAT1
    nsv4728969copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,064,955-180,719,789 , GRCh38.p12 chr5: 180,637,955-181,292,788 TMEM69P2, OR2V1, 52 more genes
    nsv4724875insertion1nstd186human GRCh37 chr5: 180,223,001-180,223,001 , GRCh38.p12 chr5: 180,796,001-180,796,001 MGAT1
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