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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv481240novel sequence insertion1nstd35human GRCh37.p13 chr1: 25,839,909-25,841,018 , chr: 21,970,329-21,971,442 , chr: 7,472,276-7,473,385 , GRCh38.p12 chr1|NT_032977.10: 24,927,430-24,928,539 0
    nsv480557novel sequence insertion1nstd35human GRCh37.p13 chr1: 25,816,168-25,816,833 , chr: 21,946,603-21,947,268 , chr: 7,448,903-7,449,568 , GRCh38.p12 chr1|NT_032977.10: 24,903,689-24,904,354 0
    nsv480374novel sequence insertion1nstd35human GRCh37.p13 chr1|NW_004070864.1: 15,555-18,479 , GRCh37.p13 chr1: 3,839,138-3,842,062 , chr: 1,514-4,442 , chr: 3,317,977-3,320,901 , GRCh38.p12 chr1|NT_032977.10: 3,336,586-3,339,510 0
    nsv480282novel sequence insertion1nstd35human GRCh37.p13 chr1: 25,878,818-25,879,771 , chr: 22,009,231-22,010,184 , chr: 22,175-23,128 , GRCh38.p12 chr1|NT_032977.10: 24,966,339-24,967,292 0
    nsv480131novel sequence insertion1nstd35human GRCh37.p13 chr1: 25,816,371-25,817,178 , chr: 21,946,806-21,947,613 , chr: 7,449,106-7,449,913 , GRCh38.p12 chr1|NT_032977.10: 24,903,892-24,904,699 0
    nsv480004novel sequence insertion1nstd35human GRCh37.p13 chr1: 28,761,038-28,761,797 , chr: 24,893,398-24,894,157 , chr: 2,659,296-2,660,055 , GRCh38.p12 chr1|NT_032977.10: 27,848,539-27,849,298 0
    nsv479886novel sequence insertion1nstd35human GRCh37.p13 chr1: 25,821,107-25,822,214 , chr: 21,951,525-21,952,632 , chr: 7,453,841-7,454,948 , GRCh38.p12 chr1|NT_032977.10: 24,908,628-24,909,735 0
    nsv479815novel sequence insertion1nstd35human GRCh37.p13 chr1: 28,753,127-28,753,920 , chr: 24,885,494-24,886,281 , chr: 2,651,382-2,652,175 , GRCh38.p12 chr1|NT_032977.10: 27,840,628-27,841,421 0
    nsv479716novel sequence insertion1nstd35human GRCh37.p13 chr1: 25,823,833-25,825,490 , chr: 21,954,251-21,955,909 , chr: 7,456,567-7,458,224 , GRCh38.p12 chr1|NT_032977.10: 24,911,354-24,913,011 0
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