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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951866insertion1nstd209human GRCh38 chr2: 168,887,421-168,887,421 , GRCh37.p13 chr2: 169,743,931-169,743,931 SPC25
    nsv5896158copy number variation1nstd209human GRCh38 chr2: 168,863,979-168,864,035 , GRCh37.p13 chr2: 169,720,489-169,720,545 NOSTRIN, SPC25
    nsv5832007copy number variation1nstd209human GRCh38 chr2: 168,867,340-168,870,073 , GRCh37.p13 chr2: 169,723,850-169,726,583 SPC25
    nsv5729697mobile element insertion1nstd211human GRCh38 chr2: 168,871,562-168,871,562 , GRCh37.p13 chr2: 169,728,072-169,728,072 SPC25
    nsv5613073insertion1nstd207human GRCh38 chr2: 168,867,268-168,867,268 , GRCh37.p13 chr2: 169,723,778-169,723,778 SPC25
    nsv5611610insertion1nstd207human GRCh38 chr2: 168,867,741-168,867,741 , GRCh37.p13 chr2: 169,724,251-169,724,251 SPC25
    nsv5605729insertion1nstd207human GRCh38 chr2: 168,889,036-168,889,036 , GRCh37.p13 chr2: 169,745,546-169,745,546 SPC25
    nsv5572850copy number variation1nstd207human GRCh38 chr2: 168,863,979-168,864,035 , GRCh37.p13 chr2: 169,720,489-169,720,545 NOSTRIN, SPC25
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453594copy number variation1nstd206human GRCh38 chr2: 168,887,883-168,888,453 , GRCh37.p13 chr2: 169,744,393-169,744,963 SPC25
    nsv5291377copy number variation1nstd204human GRCh38.p13 chr2: 168,869,484-168,876,510 , GRCh37.p13 chr2: 169,725,994-169,733,020 SPC25
    nsv5208375copy number variation1nstd204human GRCh38.p13 chr2: 168,868,330-168,876,371 , GRCh37.p13 chr2: 169,724,840-169,732,881 SPC25
    nsv5208273copy number variation1nstd204human GRCh38.p13 chr2: 168,869,501-168,876,500 , GRCh37.p13 chr2: 169,726,011-169,733,010 SPC25
    nsv5206662copy number variation1nstd204human GRCh38.p13 chr2: 168,869,364-168,875,471 , GRCh37.p13 chr2: 169,725,874-169,731,981 SPC25
    nsv5173621mobile element insertion1nstd203human GRCh38 chr2: 168,866,784-168,866,790 , GRCh37.p13 chr2: 169,723,294-169,723,300 SPC25
    nsv5079370mobile element insertion1nstd203human GRCh38 chr2: 168,869,535-168,869,551 , GRCh37.p13 chr2: 169,726,045-169,726,061 SPC25
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4928885copy number variation1nstd200human GRCh38 chr2: 168,866,057-168,869,942 , GRCh37.p13 chr2: 169,722,567-169,726,452 SPC25
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