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Items: 1 to 20 of 659

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964974insertion1nstd209human GRCh38 chr1: 948,711-948,711 , GRCh37.p13 chr1: 884,091-884,091 NOC2L
    nsv5884486copy number variation1nstd209human GRCh38 chr1: 945,428-960,875 , GRCh37.p13 chr1: 880,808-896,255 NOC2L, KLHL17
    nsv5880990copy number variation1nstd209human GRCh38 chr1: 863,087-962,195 , GRCh37.p13 chr1: 798,467-897,575 NOC2L, SAMD11, 7 more genes
    nsv5873441copy number variation1nstd209human GRCh38 chr1: 956,786-956,850 , GRCh37.p13 chr1: 892,166-892,230 NOC2L
    nsv5830817copy number variation1nstd209human GRCh38 chr1: 934,914-944,012 , GRCh37.p13 chr1: 870,294-879,392 SAMD11, NOC2L
    nsv5830546copy number variation1nstd209human GRCh38 chr1: 935,164-964,006 , GRCh37.p13 chr1: 870,544-899,386 SAMD11, PLEKHN1, 2 more genes
    nsv5432506copy number variation1nstd206human GRCh38 chr1: 950,379-950,550 , GRCh37.p13 chr1: 885,759-885,930 NOC2L
    nsv5417411copy number variation1nstd206human GRCh38 chr1: 948,661-948,730 , GRCh37.p13 chr1: 884,041-884,110 NOC2L
    nsv5341319translocation1nstd200human GRCh37 chr1: 896,256-896,256 , GRCh37 chr1: 880,808-880,808 , GRCh38.p12 chr1: 945,428-945,428 , GRCh38.p12 chr1: 960,876-960,876 NOC2L, KLHL17
    nsv5328339translocation1nstd204human GRCh37.p13 chr1: 1,052,926-1,052,926 , GRCh37.p13 chr1: 893,966-893,966 , GRCh38.p13 chr1: 1,117,546-1,117,546 , GRCh38.p13 chr1: 958,586-958,586 NOC2L, KLHL17
    nsv5217727copy number variation1nstd204human GRCh38.p13 chr1: 949,583-950,782 , GRCh37.p13 chr1: 884,963-886,162 NOC2L
    nsv5212806copy number variation1nstd204human GRCh38.p13 chr1: 958,601-1,081,700 , GRCh37.p13 chr1: 893,981-1,017,080 ISG15, NOC2L, 10 more genes
    nsv5212636copy number variation1nstd204human GRCh37.p13 chr1: 863,281-944,880 , GRCh38.p13 chr1: 927,901-1,009,500 NOC2L, HES4, 5 more genes
    nsv5211541copy number variation1nstd204human GRCh37.p13 chr1: 894,261-944,552 , GRCh38.p13 chr1: 958,881-1,009,172 NOC2L, HES4, 4 more genes
    nsv5209652copy number variation1nstd204human GRCh38.p13 chr1: 935,014-959,148 , GRCh37.p13 chr1: 870,394-894,528 SAMD11, KLHL17, 1 more genes
    nsv5208305copy number variation1nstd204human GRCh38.p13 chr1: 890,901-1,634,500 , GRCh37.p13 chr1: 826,281-1,569,876 , PLEKHN1, 62 more genes
    nsv5203371copy number variation1nstd204human GRCh38.p13 chr1: 934,001-1,382,300 , GRCh37.p13 chr1: 869,381-1,317,680 AGRN, UBE2J2, 38 more genes
    nsv4905923copy number variation1nstd200human GRCh38 chr1: 952,174-954,014 , GRCh37.p13 chr1: 887,554-889,394 NOC2L
    nsv4905922copy number variation1nstd200human GRCh38 chr1: 943,358-943,452 , GRCh37.p13 chr1: 878,738-878,832 NOC2L, SAMD11
    nsv4905921copy number variation1nstd200human GRCh38 chr1: 942,912-1,058,985 , GRCh37.p13 chr1: 878,292-994,365 HES4, PERM1, 8 more genes
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