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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869097copy number variation1nstd209human GRCh38 chr1: 185,178,737-185,178,786 , GRCh37.p13 chr1: 185,147,869-185,147,918 SWT1
    nsv5719368mobile element insertion1nstd211human GRCh38 chr1: 185,290,279-185,290,279 , GRCh37.p13 chr1: 185,259,411-185,259,411 SWT1
    nsv5680537mobile element insertion1nstd211human GRCh38 chr1: 185,269,388-185,269,388 , GRCh37.p13 chr1: 185,238,520-185,238,520 SWT1, LOC105371651
    nsv5615046insertion1nstd207human GRCh38 chr1: 185,187,062-185,187,062 , GRCh37.p13 chr1: 185,156,194-185,156,194 SWT1
    nsv5446179copy number variation1nstd206human GRCh38 chr1: 185,258,049-185,258,117 , GRCh37.p13 chr1: 185,227,181-185,227,249 SWT1
    nsv5440276copy number variation1nstd206human GRCh38 chr1: 185,178,737-185,178,787 , GRCh37.p13 chr1: 185,147,869-185,147,919 SWT1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5354072translocation1nstd200human GRCh38 chr1: 185,259,967-185,259,967 , GRCh38 chr1: 185,260,076-185,260,076 , GRCh37.p13 chr1: 185,229,208-185,229,208 , GRCh37.p13 chr1: 185,229,099-185,229,099 SWT1
    nsv5345494translocation1nstd200human GRCh37 chr1: 185,218,192-185,218,192 , GRCh37 chr1: 185,218,252-185,218,252 , GRCh38.p12 chr1: 185,249,120-185,249,120 , GRCh38.p12 chr1: 185,249,060-185,249,060 SWT1
    nsv5322350translocation1nstd204human GRCh38.p13 chr1: 185,249,063-185,249,063 , GRCh38.p13 chr1: 185,249,120-185,249,120 , GRCh37.p13 chr1: 185,218,195-185,218,195 , GRCh37.p13 chr1: 185,218,252-185,218,252 SWT1
    nsv5079208mobile element insertion1nstd203human GRCh38 chr1: 185,187,062-185,187,072 , GRCh37.p13 chr1: 185,156,194-185,156,204 SWT1
    nsv5078187mobile element insertion1nstd203human GRCh38 chr1: 185,187,072-185,187,092 , GRCh37.p13 chr1: 185,156,204-185,156,224 SWT1
    nsv5075959mobile element insertion1nstd203human GRCh38 chr1: 185,250,268-185,250,283 , GRCh37.p13 chr1: 185,219,400-185,219,415 SWT1
    nsv5073463mobile element insertion1nstd203human GRCh38 chr1: 185,187,061-185,187,072 , GRCh37.p13 chr1: 185,156,193-185,156,204 SWT1
    nsv5068236mobile element insertion1nstd203human GRCh38 chr1: 185,187,069-185,187,072 , GRCh37.p13 chr1: 185,156,201-185,156,204 SWT1
    nsv5064822mobile element insertion1nstd203human GRCh38 chr1: 185,187,027-185,187,072 , GRCh37.p13 chr1: 185,156,159-185,156,204 SWT1
    nsv5063155mobile element insertion1nstd203human GRCh38 chr1: 185,187,029-185,187,072 , GRCh37.p13 chr1: 185,156,161-185,156,204 SWT1
    nsv4906698copy number variation1nstd200human GRCh38 chr1: 185,279,294-185,285,311 , GRCh37.p13 chr1: 185,248,426-185,254,443 LOC100422414, SWT1, 1 more genes
    nsv4906697copy number variation1nstd200human GRCh38 chr1: 185,266,314-185,269,053 , GRCh37.p13 chr1: 185,235,446-185,238,185 LOC105371651, SWT1
    nsv4906696copy number variation1nstd200human GRCh38 chr1: 185,243,548-185,243,803 , GRCh37.p13 chr1: 185,212,680-185,212,935 SWT1
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