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Items: 1 to 20 of 794

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962512insertion1nstd209human GRCh38 chr2: 179,229,775-179,229,775 , GRCh37.p13 chr2: 180,094,502-180,094,502 SESTD1
    nsv5893856copy number variation1nstd209human GRCh38 chr2: 179,200,718-179,216,938 , GRCh37.p13 chr2: 180,065,445-180,081,665 SESTD1
    nsv5892877copy number variation1nstd209human GRCh38 chr2: 179,099,600-179,106,757 , GRCh37.p13 chr2: 179,964,327-179,971,484 SESTD1
    nsv5832031copy number variation1nstd209human GRCh38 chr2: 179,200,691-179,216,706 , GRCh37.p13 chr2: 180,065,418-180,081,433 SESTD1
    nsv5831761copy number variation1nstd209human GRCh38 chr2: 179,099,572-179,106,815 , GRCh37.p13 chr2: 179,964,299-179,971,542 SESTD1
    nsv5690631mobile element insertion1nstd211human GRCh38 chr2: 179,116,900-179,116,900 , GRCh37.p13 chr2: 179,981,627-179,981,627 SESTD1
    nsv5688743mobile element insertion1nstd211human GRCh38 chr2: 179,255,055-179,255,055 , GRCh37.p13 chr2: 180,119,782-180,119,782 SESTD1
    nsv5687872mobile element insertion1nstd211human GRCh38 chr2: 179,235,561-179,235,561 , GRCh37.p13 chr2: 180,100,288-180,100,288 SESTD1
    nsv5684472mobile element insertion2nstd211human GRCh38 chr2: 179,175,875-179,175,875 , GRCh37.p13 chr2: 180,040,602-180,040,602 SESTD1
    nsv5679398mobile element insertion1nstd211human GRCh38 chr2: 179,237,078-179,237,078 , GRCh37.p13 chr2: 180,101,805-180,101,805 SESTD1
    nsv5615579insertion1nstd207human GRCh38 chr2: 179,259,034-179,259,034 , GRCh37.p13 chr2: 180,123,761-180,123,761 SESTD1
    nsv5610059insertion1nstd207human GRCh38 chr2: 179,185,684-179,185,684 , GRCh37.p13 chr2: 180,050,411-180,050,411 SESTD1
    nsv5607592insertion1nstd207human GRCh38 chr2: 179,131,082-179,131,082 , GRCh37.p13 chr2: 179,995,809-179,995,809 SESTD1
    nsv5583507copy number variation1nstd207human GRCh38 chr2: 179,185,785-179,185,864 , GRCh37.p13 chr2: 180,050,512-180,050,591 SESTD1
    nsv5580591copy number variation1nstd207human GRCh38 chr2: 179,200,620-179,216,830 , GRCh37.p13 chr2: 180,065,347-180,081,557 SESTD1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5549196insertion1nstd206human GRCh38 chr2: 179,185,585-179,185,585 , GRCh37.p13 chr2: 180,050,312-180,050,312 SESTD1
    nsv5449981copy number variation1nstd206human GRCh38 chr2: 179,114,823-179,114,897 , GRCh37.p13 chr2: 179,979,550-179,979,624 SESTD1
    nsv5436249copy number variation1nstd206human GRCh38 chr2: 179,087,618-179,100,000 , GRCh37.p13 chr2: 179,952,345-179,964,727 SESTD1
    nsv5435916copy number variation1nstd206human GRCh38 chr2: 179,099,603-179,106,758 , GRCh37.p13 chr2: 179,964,330-179,971,485 SESTD1
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