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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869406copy number variation1nstd209human GRCh38 chr1: 160,844,784-160,844,946 , GRCh37.p13 chr1: 160,814,574-160,814,736 CD244
    nsv5690720mobile element insertion1nstd211human GRCh38 chr1: 160,840,025-160,840,025 , GRCh37.p13 chr1: 160,809,815-160,809,815 CD244
    nsv5413275mobile element insertion1nstd206human GRCh38 chr1: 160,840,025-160,840,076 , GRCh37.p13 chr1: 160,809,815-160,809,866 CD244
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5069554mobile element insertion1nstd203human GRCh38 chr1: 160,840,009-160,840,025 , GRCh37.p13 chr1: 160,809,799-160,809,815 CD244
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4683645copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,786,670-161,332,308 , GRCh38.p12 chr1: 160,816,880-161,362,518 PCP4L1, NECTIN4, 32 more genes
    nsv4579666copy number variation1nstd183human GRCh37 chr1: 160,827,227-160,870,106 , GRCh38.p12 chr1: 160,857,437-160,900,316 CD244, ITLN1, 1 more genes
    nsv4518029copy number variation1nstd166human GRCh37.p13 chr1: 160,818,699-161,386,000 , GRCh38.p12 chr1: 160,848,909-161,416,210 LOC101928372, LOC107985221, 37 more genes
    nsv4459040mobile element insertion1nstd166human GRCh37.p13 chr1: 160,801,953-160,801,953 , GRCh38.p12 chr1: 160,832,163-160,832,163 CD244
    nsv4452657copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,744,174-162,583,871 , GRCh38.p12 chr1: 160,774,384-162,614,081 TRD-GTC2-2, KLHDC9, 104 more genes
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4450321copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,808,188-161,011,163 , GRCh38.p12 chr1: 159,838,398-161,041,373 LOC107985216, PPIAP37, 50 more genes
    nsv4450213copy number variation1nstd102humanUncertain significance GRCh38 chr1: 160,816,880-161,362,443 , GRCh37 chr1: 160,786,670-161,332,233 ADAMTS4, TOMM40L, 32 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 LINC00626, RN7SL861P, 359 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4326779sequence alteration1nstd166human GRCh37.p13 chr1: 160,775,738-160,870,422 , GRCh38.p12 chr1: 160,805,948-160,900,632 LY9, CD244, 3 more genes
    nsv3966913copy number variation1nstd168human GRCh38 chr1: 160,820,525-160,839,881 , GRCh37.p13 chr1: 160,790,315-160,809,671 LY9, CD244
    nsv3965619insertion1nstd168human GRCh38 chr1: 160,799,359-160,836,422 , GRCh37.p13 chr1: 160,769,149-160,806,212 LY9, CD244
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