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Items: 1 to 20 of 160

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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
    nsv5899834copy number variation1nstd209human GRCh38 chr3: 126,417,493-126,440,291 , GRCh37.p13 chr3: 126,136,336-126,159,134 ZXDC, CFAP100
    nsv5691763mobile element insertion1nstd211human GRCh38 chr3: 126,401,443-126,401,443 , GRCh37.p13 chr3: 126,120,286-126,120,286 CFAP100
    nsv5453256copy number variation1nstd206human GRCh38 chr3: 126,423,018-126,424,325 , GRCh37.p13 chr3: 126,141,861-126,143,168 CFAP100
    nsv5449206copy number variation1nstd206human GRCh38 chr3: 126,422,988-126,423,355 , GRCh37.p13 chr3: 126,141,831-126,142,198 CFAP100
    nsv5436395copy number variation1nstd206human GRCh38 chr3: 126,401,398-126,401,452 , GRCh37.p13 chr3: 126,120,241-126,120,295 CFAP100
    nsv5435850copy number variation1nstd206human GRCh38 chr3: 126,435,153-126,440,210 , GRCh37.p13 chr3: 126,153,996-126,159,053 CFAP100, ZXDC
    nsv5434580copy number variation1nstd206human GRCh38 chr3: 126,397,314-126,397,483 , GRCh37.p13 chr3: 126,116,157-126,116,326 CFAP100
    nsv5096258mobile element insertion1nstd203human GRCh38 chr3: 126,411,361-126,411,387 , GRCh37.p13 chr3: 126,130,204-126,130,230 CFAP100
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914725copy number variation1nstd200human GRCh38 chr3: 126,399,673-126,399,963 , GRCh37.p13 chr3: 126,118,516-126,118,806 CFAP100
    nsv4596021copy number variation1nstd183human GRCh37 chr3: 126,141,934-126,142,572 , GRCh38.p12 chr3: 126,423,091-126,423,729 CFAP100
    nsv4584713copy number variation1nstd183human GRCh37 chr3: 126,138,905-126,139,078 , GRCh38.p12 chr3: 126,420,062-126,420,235 CFAP100
    nsv4520441copy number variation1nstd166human GRCh37.p13 chr3: 125,973,998-126,178,000 , GRCh38.p12 chr3: 126,255,155-126,459,157 KLF15, ZXDC, 5 more genes
    nsv4468957mobile element insertion1nstd166human GRCh37.p13 chr3: 126,114,799-126,114,799 , GRCh38.p12 chr3: 126,395,956-126,395,956 CFAP100
    nsv4368647copy number variation1nstd173human GRCh37 chr3: 125,803,412-126,619,202 , GRCh38.p12 chr3: 126,084,569-126,900,359 CFAP100-DT, RCC2P4, 24 more genes
    nsv4347357copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 124,369,671-126,423,192 , GRCh38.p12 chr3: 124,650,824-126,704,349 ITGB5, UMPS, 63 more genes
    nsv4090538copy number variation1nstd166human GRCh37.p13 chr3: 126,131,886-126,131,949 , GRCh38.p12 chr3: 126,413,043-126,413,106 CFAP100
    nsv4081466copy number variation1nstd166human GRCh37.p13 chr3: 126,117,840-126,119,154 , GRCh38.p12 chr3: 126,398,997-126,400,311 CFAP100
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