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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5931738copy number variation1nstd209human GRCh38 chr13: 40,661,542-40,661,624 , GRCh37.p13 chr13: 41,235,679-41,235,761 FOXO1
    nsv5711012mobile element insertion2nstd211human GRCh38 chr13: 40,566,819-40,566,819 , GRCh37.p13 chr13: 41,140,956-41,140,956 FOXO1
    nsv5699783mobile element insertion2nstd211human GRCh38 chr13: 40,568,630-40,568,630 , GRCh37.p13 chr13: 41,142,767-41,142,767 FOXO1
    nsv5697695mobile element insertion2nstd211human GRCh38 chr13: 40,631,327-40,631,327 , GRCh37.p13 chr13: 41,205,464-41,205,464 FOXO1
    nsv5696084mobile element insertion1nstd211human GRCh38 chr13: 40,574,188-40,574,188 , GRCh37.p13 chr13: 41,148,325-41,148,325 FOXO1
    nsv5646477insertion1nstd207human GRCh38 chr13: 40,617,347-40,617,347 , GRCh37.p13 chr13: 41,191,484-41,191,484 RLIMP1, FOXO1
    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
    nsv5500466copy number variation1nstd206human GRCh38 chr13: 40,661,542-40,661,625 , GRCh37.p13 chr13: 41,235,679-41,235,762 FOXO1
    nsv5433769mobile element insertion1nstd206human GRCh38 chr13: 40,631,327-40,631,378 , GRCh37.p13 chr13: 41,205,464-41,205,515 FOXO1
    nsv5424146mobile element insertion1nstd206human GRCh38 chr13: 40,568,630-40,568,681 , GRCh37.p13 chr13: 41,142,767-41,142,818 FOXO1
    nsv5418392mobile element insertion1nstd206human GRCh38 chr13: 40,566,819-40,566,870 , GRCh37.p13 chr13: 41,140,956-41,141,007 FOXO1
    nsv5311559copy number variation1nstd204human GRCh37.p13 chr13: 41,190,616-41,208,324 , GRCh38.p13 chr13: 40,616,479-40,634,187 RLIMP1, FOXO1
    nsv5279822copy number variation1nstd204human GRCh38.p13 chr13: 40,616,771-40,634,222 , GRCh37.p13 chr13: 41,190,908-41,208,359 RLIMP1, FOXO1
    nsv5271408copy number variation1nstd204human GRCh38.p13 chr13: 40,618,608-40,619,807 , GRCh37.p13 chr13: 41,192,745-41,193,944 FOXO1, RLIMP1
    nsv5271206copy number variation1nstd204human GRCh38.p13 chr13: 40,622,808-40,624,145 , GRCh37.p13 chr13: 41,196,945-41,198,282 FOXO1
    nsv5157812mobile element insertion1nstd203human GRCh38 chr13: 40,582,171-40,582,186 , GRCh37.p13 chr13: 41,156,308-41,156,323 FOXO1
    nsv5157220mobile element insertion1nstd203human GRCh38 chr13: 40,574,173-40,574,188 , GRCh37.p13 chr13: 41,148,310-41,148,325 FOXO1
    nsv5146242mobile element insertion1nstd203human GRCh38 chr13: 40,574,176-40,574,188 , GRCh37.p13 chr13: 41,148,313-41,148,325 FOXO1
    nsv4997133copy number variation1nstd200human GRCh38 chr13: 40,623,856-40,632,686 , GRCh37.p13 chr13: 41,197,993-41,206,823 FOXO1
    nsv4997132copy number variation1nstd200human GRCh38 chr13: 40,570,615-40,572,864 , GRCh37.p13 chr13: 41,144,752-41,147,001 FOXO1
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