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Items: 1 to 20 of 316

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905103copy number variation1nstd209human GRCh38 chr4: 70,910,228-70,916,747 , GRCh37.p13 chr4: 71,775,945-71,782,464 MOB1B
    nsv5902813copy number variation1nstd209human GRCh38 chr4: 70,936,541-70,939,033 , GRCh37.p13 chr4: 71,802,258-71,804,750 MOB1B
    nsv5895242copy number variation1nstd209human GRCh38 chr4: 70,987,038-70,989,257 , GRCh37.p13 chr4: 71,852,755-71,854,974 MOB1B
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5840047copy number variation1nstd209human GRCh38 chr4: 70,936,351-70,938,450 , GRCh37.p13 chr4: 71,802,068-71,804,167 MOB1B
    nsv5839477copy number variation1nstd209human GRCh38 chr4: 70,911,489-70,916,740 , GRCh37.p13 chr4: 71,777,206-71,782,457 MOB1B
    nsv5719668mobile element insertion1nstd211human GRCh38 chr4: 70,919,428-70,919,428 , GRCh37.p13 chr4: 71,785,145-71,785,145 MOB1B
    nsv5692270mobile element insertion1nstd211human GRCh38 chr4: 70,901,472-70,901,472 , GRCh37.p13 chr4: 71,767,189-71,767,189 MOB1B
    nsv5685001mobile element insertion2nstd211human GRCh38 chr4: 70,985,050-70,985,050 , GRCh37.p13 chr4: 71,850,767-71,850,767 MOB1B
    nsv5678240mobile element insertion1nstd211human GRCh38 chr4: 70,905,767-70,905,767 , GRCh37.p13 chr4: 71,771,484-71,771,484 MOB1B
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5471633copy number variation1nstd206human GRCh38 chr4: 70,933,721-70,934,665 , GRCh37.p13 chr4: 71,799,438-71,800,382 MOB1B
    nsv5466133copy number variation1nstd206human GRCh38 chr4: 70,935,667-70,935,742 , GRCh37.p13 chr4: 71,801,384-71,801,459 MOB1B
    nsv5465927copy number variation1nstd206human GRCh38 chr4: 70,902,293-70,904,257 , GRCh37.p13 chr4: 71,768,010-71,769,974 MOB1B
    nsv5464733copy number variation1nstd206human GRCh38 chr4: 70,936,541-70,939,034 , GRCh37.p13 chr4: 71,802,258-71,804,751 MOB1B
    nsv5413753mobile element insertion1nstd206human GRCh38 chr4: 70,905,767-70,905,818 , GRCh37.p13 chr4: 71,771,484-71,771,535 MOB1B
    nsv5408083mobile element insertion1nstd206human GRCh38 chr4: 70,985,050-70,985,101 , GRCh37.p13 chr4: 71,850,767-71,850,818 MOB1B
    nsv5346700translocation1nstd200human GRCh38 chr4: 70,939,034-70,939,034 , GRCh38 chr4: 70,936,541-70,936,541 , GRCh37.p13 chr4: 71,802,258-71,802,258 , GRCh37.p13 chr4: 71,804,751-71,804,751 MOB1B
    nsv5312049copy number variation1nstd204human GRCh38.p13 chr4: 70,954,103-70,954,187 , GRCh37.p13 chr4: 71,819,820-71,819,904 MOB1B
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