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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5908721copy number variation1nstd209human GRCh38 chr7: 140,427,416-140,429,155 , GRCh37.p13 chr7: 140,127,216-140,128,955 RAB19
    nsv5861510copy number variation1nstd209human GRCh38 chr7: 140,427,398-140,429,149 , GRCh37.p13 chr7: 140,127,198-140,128,949 RAB19
    nsv5697807mobile element insertion2nstd211human GRCh38 chr7: 140,402,315-140,402,315 , GRCh37.p13 chr7: 140,102,115-140,102,115 RAB19
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5492326copy number variation1nstd206human GRCh38 chr7: 140,405,917-140,406,271 , GRCh37.p13 chr7: 140,105,717-140,106,071 RAB19
    nsv5488933copy number variation1nstd206human GRCh38 chr7: 140,413,560-140,416,103 , GRCh37.p13 chr7: 140,113,360-140,115,903 RAB19
    nsv5486862copy number variation1nstd206human GRCh38 chr7: 140,427,752-140,428,600 , GRCh37.p13 chr7: 140,127,552-140,128,400 RAB19
    nsv5486269copy number variation1nstd206human GRCh38 chr7: 140,409,776-140,411,182 , GRCh37.p13 chr7: 140,109,576-140,110,982 RAB19
    nsv5484501copy number variation1nstd206human GRCh38 chr7: 140,402,142-140,403,658 , GRCh37.p13 chr7: 140,101,942-140,103,458 RAB19
    nsv5407150mobile element insertion1nstd206human GRCh38 chr7: 140,402,315-140,402,341 , GRCh37.p13 chr7: 140,102,115-140,102,141 RAB19
    nsv5371294translocation1nstd200human GRCh38 chr7: 140,416,080-140,416,080 , GRCh38 chr7: 140,413,583-140,413,583 , GRCh37.p13 chr7: 140,115,880-140,115,880 , GRCh37.p13 chr7: 140,113,383-140,113,383 RAB19
    nsv5371293translocation1nstd200human GRCh38 chr7: 140,416,070-140,416,070 , GRCh38 chr7: 140,413,294-140,413,294 , GRCh37.p13 chr7: 140,115,870-140,115,870 , GRCh37.p13 chr7: 140,113,094-140,113,094 RAB19
    nsv5333210translocation1nstd200human GRCh37 chr7: 140,115,870-140,115,870 , GRCh37 chr7: 140,113,094-140,113,094 , GRCh38.p12 chr7: 140,413,294-140,413,294 , GRCh38.p12 chr7: 140,416,070-140,416,070 RAB19
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5310279copy number variation1nstd204human GRCh38.p13 chr7: 140,413,291-140,416,075 , GRCh37.p13 chr7: 140,113,091-140,115,875 RAB19
    nsv5308548copy number variation1nstd204human GRCh38.p13 chr7: 140,363,195-140,432,767 , GRCh37.p13 chr7: 140,062,995-140,132,567 RNA5SP248, SLC37A3, 2 more genes
    nsv5252012copy number variation1nstd204human GRCh38.p13 chr7: 140,402,550-140,403,749 , GRCh37.p13 chr7: 140,102,350-140,103,549 RAB19
    nsv5251046copy number variation1nstd204human GRCh38.p13 chr7: 140,413,301-140,416,210 , GRCh37.p13 chr7: 140,113,101-140,116,010 RAB19
    nsv5246399copy number variation1nstd204human GRCh38.p13 chr7: 140,360,222-140,430,318 , GRCh37.p13 chr7: 140,060,022-140,130,118 RNA5SP247, SLC37A3, 2 more genes
    nsv5245009copy number variation1nstd204human GRCh38.p13 chr7: 140,427,601-140,432,300 , GRCh37.p13 chr7: 140,127,401-140,132,100 RAB19
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