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Items: 1 to 20 of 187

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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
    nsv5897978copy number variation1nstd209human GRCh38 chr3: 127,387,819-127,387,869 , GRCh37.p13 chr3: 127,106,662-127,106,712 LOC105374094, LINC02016
    nsv5890686copy number variation1nstd209human GRCh38 chr3: 127,373,559-127,373,706 , GRCh37.p13 chr3: 127,092,402-127,092,549 LINC02016
    nsv5622308insertion1nstd207human GRCh38 chr3: 127,387,629-127,387,629 , GRCh37.p13 chr3: 127,106,472-127,106,472 LOC105374094, LINC02016
    nsv5575176copy number variation1nstd207human GRCh38 chr3: 127,387,819-127,387,869 , GRCh37.p13 chr3: 127,106,662-127,106,712 LINC02016, LOC105374094
    nsv5569759copy number variation1nstd207human GRCh38 chr3: 127,373,069-127,373,175 , GRCh37.p13 chr3: 127,091,912-127,092,018 LINC02016
    nsv5538608insertion1nstd206human GRCh38 chr3: 127,344,313-127,344,313 , GRCh37.p13 chr3: 127,063,156-127,063,156 LINC02016
    nsv5444694copy number variation1nstd206human GRCh38 chr3: 127,368,994-127,369,167 , GRCh37.p13 chr3: 127,087,837-127,088,010 LINC02016
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919975copy number variation1nstd200human GRCh38 chr3: 127,249,957-127,325,345 , GRCh37.p13 chr3: 126,968,800-127,044,188 PRR20G, LINC02016
    nsv4914731copy number variation1nstd200human GRCh38 chr3: 127,368,994-127,369,167 , GRCh37.p13 chr3: 127,087,837-127,088,010 LINC02016
    nsv4678988copy number variation1nstd189human GRCh37.p13 chr3: 126,832,331-127,070,201 , GRCh38.p12 chr3: 127,113,488-127,351,358 PRR23E, PRR20G, 3 more genes
    nsv4584791copy number variation1nstd183human GRCh37 chr3: 127,058,811-127,231,663 , GRCh38.p12 chr3: 127,339,968-127,512,820 LOC105374094, LINC02016, 1 more genes
    nsv4468959mobile element insertion1nstd166human GRCh37.p13 chr3: 127,088,138-127,088,138 , GRCh38.p12 chr3: 127,369,295-127,369,295 LINC02016
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4110528copy number variation1nstd166human GRCh37.p13 chr3: 127,070,820-127,070,912 , GRCh38.p12 chr3: 127,351,977-127,352,069 LINC02016
    nsv4105937copy number variation1nstd166human GRCh37.p13 chr3: 127,087,837-127,088,010 , GRCh38.p12 chr3: 127,368,994-127,369,167 LINC02016
    nsv4102326copy number variation1nstd166human GRCh37.p13 chr3: 127,106,412-127,106,507 , GRCh38.p12 chr3: 127,387,569-127,387,664 LINC02016, LOC105374094
    nsv4100045copy number variation1nstd166human GRCh37.p13 chr3: 127,085,483-127,090,125 , GRCh38.p12 chr3: 127,366,640-127,371,282 LINC02016
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