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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7095561copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,918-168,282,240 , GRCh38.p12 chr1: 167,431,681-168,313,002 GCSHP5, RNU6-1310P, 21 more genes
    nsv6644264copy number variation1nstd229human GRCh38 chr1: 168,249,758-168,263,426 , GRCh37.p13 chr1: 168,218,996-168,232,664 SFT2D2, RNU6-1310P
    nsv6644263copy number variation1nstd229human GRCh38 chr1: 168,239,161-168,242,498 , GRCh37.p13 chr1: 168,208,399-168,211,736 SFT2D2
    nsv6644262copy number variation1nstd229human GRCh38 chr1: 168,236,774-168,242,499 , GRCh37.p13 chr1: 168,206,012-168,211,737 SFT2D2
    nsv6644261copy number variation1nstd229human GRCh38 chr1: 168,231,909-168,410,386 , GRCh37.p13 chr1: 168,201,147-168,379,624 MIR557, SFT2D2, 5 more genes
    nsv6644258copy number variation1nstd229human GRCh38 chr1: 168,191,501-168,243,300 , GRCh37.p13 chr1: 168,160,739-168,212,538 RPL34P1, LOC107985453, 2 more genes
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644209copy number variation1nstd229human GRCh38 chr1: 168,253,017-168,265,334 , GRCh37.p13 chr1: 168,222,255-168,234,572 SFT2D2, RNU6-1310P
    nsv6644207copy number variation1nstd229human GRCh38 chr1: 168,180,838-168,254,478 , GRCh37.p13 chr1: 168,150,076-168,223,716 TIPRL, SFT2D2, 3 more genes
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6324043copy number variation1nstd223human GRCh38 chr1: 168,222,914-168,227,111 , GRCh37.p13 chr1: 168,192,152-168,196,349 SFT2D2
    nsv6322493copy number variation1nstd223human GRCh38 chr1: 168,231,902-168,410,441 , GRCh37.p13 chr1: 168,201,140-168,379,679 ANKRD36BP1, RNU6-1310P, 5 more genes
    nsv6320986copy number variation1nstd223human GRCh38 chr1: 168,253,016-168,265,330 , GRCh37.p13 chr1: 168,222,254-168,234,568 RNU6-1310P, SFT2D2
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6133937copy number variation1nstd213human GRCh37 chr1: 167,800,000-169,660,001 , GRCh38.p12 chr1: 167,830,762-169,690,860 XCL2, TBX19, 38 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133597copy number variation1nstd213human GRCh37 chr1: 167,470,000-170,370,001 , GRCh38.p12 chr1: 167,500,763-170,400,860 CD247, XCL1, 64 more genes
    nsv6133565copy number variation1nstd213human GRCh37 chr1: 164,310,000-170,640,001 , GRCh38.p12 chr1: 164,340,763-170,670,860 ATP1B1, DPT, 126 more genes
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