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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv481381novel sequence insertion1nstd35human GRCh37.p13 chr7|NW_003871065.1: 232,736-233,595 , chr: 1,099,483-1,100,342 , GRCh38.p12 chr7|NT_007933.16: 68,046,734-68,047,593 0
    nsv481280novel sequence insertion1nstd35human GRCh37.p13 chr7|NW_003871065.1: 238,892-239,672 , chr: 1,093,406-1,094,186 , GRCh38.p12 chr7|NT_007933.16: 68,052,882-68,053,662 0
    nsv481187novel sequence insertion1nstd35human GRCh38.p12 chr7|NT_007933.16: 68,027,966-68,028,806 0
    nsv480906novel sequence insertion1nstd35human chr: 1,134,228-1,136,416 , GRCh38.p12 chr7|NT_007933.16: 68,009,017-68,011,204 0
    nsv480535novel sequence insertion1nstd35human GRCh37.p13 chr7|NW_003871065.1: 239,920-241,108 , chr: 1,091,970-1,093,158 , GRCh38.p12 chr7|NT_007933.16: 68,053,910-68,055,098 0
    nsv480303novel sequence insertion1nstd35human GRCh37.p13 chr7|NW_003871065.1: 242,949-243,717 , chr: 1,089,361-1,090,129 , GRCh38.p12 chr7|NT_007933.16: 68,056,939-68,057,707 0
    nsv480128novel sequence insertion1nstd35human GRCh37.p13 chr7|NW_003871065.1: 228,470-229,275 , chr: 1,103,803-1,104,608 , GRCh38.p12 chr7|NT_007933.16: 68,042,469-68,043,274 0
    nsv479573novel sequence insertion1nstd35human GRCh37.p13 chr7|NW_003571041.1: 127,447-129,969 , chr: 463,162-465,685 , GRCh38.p12 chr7|NT_007933.16: 36,251,486-36,254,008 0
    nsv479326novel sequence insertion1nstd35human GRCh37.p13 chr7: 155,121,381-155,122,647 , chr: 4,016,355-4,017,621 , chr: 750,324-751,590 , GRCh38.p12 chr7|NT_007933.16: 92,822,892-92,824,158 0
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