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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5904628copy number variation1nstd209human GRCh38 chr3: 127,643,961-127,644,038 , GRCh37.p13 chr3: 127,362,804-127,362,881 PODXL2
    nsv5610807insertion1nstd207human GRCh38 chr3: 127,662,768-127,662,768 , GRCh37.p13 chr3: 127,381,611-127,381,611 PODXL2
    nsv5451287copy number variation1nstd206human GRCh38 chr3: 127,640,992-127,641,077 , GRCh37.p13 chr3: 127,359,835-127,359,920 PODXL2
    nsv5449143copy number variation1nstd206human GRCh38 chr3: 127,647,470-127,647,670 , GRCh37.p13 chr3: 127,366,313-127,366,513 PODXL2
    nsv5443440copy number variation1nstd206human GRCh38 chr3: 127,643,961-127,644,042 , GRCh37.p13 chr3: 127,362,804-127,362,885 PODXL2
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919986copy number variation1nstd200human GRCh38 chr3: 127,640,591-127,642,183 , GRCh37.p13 chr3: 127,359,434-127,361,026 PODXL2
    nsv4807092copy number variation1nstd200human GRCh37 chr3: 127,362,804-127,362,885 , GRCh38.p12 chr3: 127,643,961-127,644,042 PODXL2
    nsv4807091copy number variation1nstd200human GRCh37 chr3: 127,359,434-127,361,026 , GRCh38.p12 chr3: 127,640,591-127,642,183 PODXL2
    nsv4680096copy number variation1nstd189human GRCh37.p13 chr3: 127,370,661-127,593,048 , GRCh38.p12 chr3: 127,651,818-127,874,205 MGLL, PODXL2, 4 more genes
    nsv4587218copy number variation1nstd183human GRCh37 chr3: 127,347,693-127,348,493 , GRCh38.p12 chr3: 127,628,850-127,629,650 PODXL2, LOC107986126
    nsv4561644sequence alteration1nstd166human GRCh37.p13 chr3: 127,355,438-127,355,903 , GRCh38.p12 chr3: 127,636,595-127,637,060 PODXL2
    nsv4403564copy number variation1nstd174human GRCh37 chr3: 127,347,693-127,348,493 , GRCh38.p12 chr3: 127,628,850-127,629,650 PODXL2, LOC107986126
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4108095copy number variation1nstd166human GRCh37.p13 chr3: 127,359,835-127,359,920 , GRCh38.p12 chr3: 127,640,992-127,641,077 PODXL2
    nsv4104199copy number variation1nstd166human GRCh37.p13 chr3: 127,362,804-127,362,885 , GRCh38.p12 chr3: 127,643,961-127,644,042 PODXL2
    nsv3971060insertion1nstd168human GRCh38 chr3: 127,594,938-127,631,017 , GRCh37.p13 chr3: 127,313,781-127,349,860 MCM2, PODXL2, 2 more genes
    nsv3923961copy number variation1nstd102humanPathogenic GRCh38 chr3: 126,797,420-128,946,623 , GRCh37 chr3: 126,516,263-128,665,466 , NCBI36 chr3: 127,998,953-130,148,156 RUVBL1-AS1, LOC105374096, 49 more genes
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