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Items: 1 to 20 of 362

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962668insertion1nstd209human GRCh38 chr1: 99,907,693-99,907,693 , GRCh37.p13 chr1: 100,373,249-100,373,249 AGL
    nsv5954806insertion1nstd209human GRCh38 chr1: 99,890,342-99,890,342 , GRCh37.p13 chr1: 100,355,898-100,355,898 AGL
    nsv5883649copy number variation1nstd209human GRCh38 chr1: 99,850,806-99,850,880 , GRCh37.p13 chr1: 100,316,362-100,316,436 AGL
    nsv5880799copy number variation1nstd209human GRCh38 chr1: 99,854,031-99,855,637 , GRCh37.p13 chr1: 100,319,587-100,321,193 AGL
    nsv5878921copy number variation1nstd209human GRCh38 chr1: 99,856,995-99,857,121 , GRCh37.p13 chr1: 100,322,551-100,322,677 AGL
    nsv5878329copy number variation1nstd209human GRCh38 chr1: 99,874,614-99,874,681 , GRCh37.p13 chr1: 100,340,170-100,340,237 AGL
    nsv5877200copy number variation1nstd209human GRCh38 chr1: 99,917,990-99,918,116 , GRCh37.p13 chr1: 100,383,546-100,383,672 AGL
    nsv5874369copy number variation1nstd209human GRCh38 chr1: 99,903,816-99,904,328 , GRCh37.p13 chr1: 100,369,372-100,369,884 AGL
    nsv5869546copy number variation1nstd209human GRCh38 chr1: 99,816,256-99,858,185 , GRCh37.p13 chr1: 100,281,812-100,323,741 RPL39P9, AGL
    nsv5868578copy number variation1nstd209human GRCh38 chr1: 99,899,462-99,899,833 , GRCh37.p13 chr1: 100,365,018-100,365,389 AGL
    nsv5830561copy number variation1nstd209human GRCh38 chr1: 99,835,737-99,856,672 , GRCh37.p13 chr1: 100,301,293-100,322,228 AGL, RPL39P9
    nsv5687946mobile element insertion2nstd211human GRCh38 chr1: 99,890,384-99,890,384 , GRCh37.p13 chr1: 100,355,940-100,355,940 AGL
    nsv5684389mobile element insertion1nstd211human GRCh38 chr1: 99,866,803-99,866,803 , GRCh37.p13 chr1: 100,332,359-100,332,359 AGL
    nsv5680535mobile element insertion1nstd211human GRCh38 chr1: 99,877,181-99,877,181 , GRCh37.p13 chr1: 100,342,737-100,342,737 AGL
    nsv5675734mobile element insertion1nstd211human GRCh38 chr1: 99,862,154-99,862,154 , GRCh37.p13 chr1: 100,327,710-100,327,710 AGL
    nsv5674300insertion1nstd102humanPathogenic GRCh37 chr1: 100,381,024-100,381,024 , GRCh38 chr1: 99,915,468-99,915,468 AGL
    nsv5673238copy number variation1nstd102humanPathogenic GRCh37 chr1: 100,340,233-100,343,394 , GRCh38.p12 chr1: 99,874,677-99,877,838 AGL
    nsv5614017insertion1nstd207human GRCh38 chr1: 99,890,378-99,890,378 , GRCh37.p13 chr1: 100,355,934-100,355,934 AGL
    nsv5606044insertion1nstd207human GRCh38 chr1: 99,874,634-99,874,634 , GRCh37.p13 chr1: 100,340,190-100,340,190 AGL
    nsv5557277sequence alteration1nstd206human GRCh38 chr1: 99,849,753-99,849,771 , GRCh37.p13 chr1: 100,315,309-100,315,327 AGL
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