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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116635mobile element insertion1nstd186human GRCh37 chr13: 37,568,754-37,568,798 , GRCh38.p12 chr13: 36,994,617-36,994,661 ALG5
    nsv5972412insertion1nstd209human GRCh38 chr13: 36,994,603-36,994,603 , GRCh37.p13 chr13: 37,568,740-37,568,740 ALG5
    nsv5696972mobile element insertion2nstd211human GRCh38 chr13: 36,994,617-36,994,617 , GRCh37.p13 chr13: 37,568,754-37,568,754 ALG5
    nsv5695526mobile element insertion2nstd211human GRCh38 chr13: 36,991,347-36,991,347 , GRCh37.p13 chr13: 37,565,484-37,565,484 ALG5
    nsv5651794insertion1nstd207human GRCh38 chr13: 36,991,330-36,991,330 , GRCh37.p13 chr13: 37,565,467-37,565,467 ALG5
    nsv5650476insertion1nstd207human GRCh38 chr13: 36,994,603-36,994,603 , GRCh37.p13 chr13: 37,568,740-37,568,740 ALG5
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5432700mobile element insertion1nstd206human GRCh38 chr13: 36,994,617-36,994,661 , GRCh37.p13 chr13: 37,568,754-37,568,798 ALG5
    nsv5421838mobile element insertion1nstd206human GRCh38 chr13: 36,991,347-36,991,370 , GRCh37.p13 chr13: 37,565,484-37,565,507 ALG5
    nsv5158595mobile element insertion1nstd203human GRCh38 chr13: 36,991,329-36,991,345 , GRCh37.p13 chr13: 37,565,466-37,565,482 ALG5
    nsv5158220mobile element insertion1nstd203human GRCh38 chr13: 36,994,610-36,994,617 , GRCh37.p13 chr13: 37,568,747-37,568,754 ALG5
    nsv5157313mobile element insertion1nstd203human GRCh38 chr13: 36,994,608-36,994,617 , GRCh37.p13 chr13: 37,568,745-37,568,754 ALG5
    nsv5151366mobile element insertion1nstd203human GRCh38 chr13: 36,991,330-36,991,347 , GRCh37.p13 chr13: 37,565,467-37,565,484 ALG5
    nsv5145708mobile element insertion1nstd203human GRCh38 chr13: 36,994,609-36,994,617 , GRCh37.p13 chr13: 37,568,746-37,568,754 ALG5
    nsv5144067mobile element insertion1nstd203human GRCh38 chr13: 36,994,603-36,994,617 , GRCh37.p13 chr13: 37,568,740-37,568,754 ALG5
    nsv5004456copy number variation1nstd200human GRCh38 chr13: 31,196,586-38,438,583 , GRCh37.p13 chr13: 31,770,723-39,012,720 , LOC102723490, 82 more genes
    nsv4997001copy number variation1nstd200human GRCh38 chr13: 36,976,494-36,976,596 , GRCh37.p13 chr13: 37,550,631-37,550,733 ALG5
    nsv4717486mobile element insertion1nstd186human GRCh37 chr13: 37,565,467-37,565,467 , GRCh38.p12 chr13: 36,991,330-36,991,330 ALG5
    nsv4716621mobile element insertion1nstd186human GRCh37 chr13: 37,568,740-37,568,740 , GRCh38.p12 chr13: 36,994,603-36,994,603 ALG5
    nsv4689583mobile element insertion1nstd186human GRCh37 chr13: 37,568,754-37,568,754 , GRCh38.p12 chr13: 36,994,617-36,994,617 ALG5
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