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Items: 1 to 20 of 325

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118805copy number variation1nstd186human GRCh37 chr2: 120,417,079-120,418,495 , GRCh38.p12 chr2: 119,659,503-119,660,919 CFAP221
    nsv5900158copy number variation1nstd209human GRCh38 chr2: 119,659,621-119,660,918 , GRCh37.p13 chr2: 120,417,197-120,418,494 CFAP221
    nsv5897296copy number variation1nstd209human GRCh38 chr2: 119,659,503-119,660,911 , GRCh37.p13 chr2: 120,417,079-120,418,487 CFAP221
    nsv5831122copy number variation1nstd209human GRCh38 chr2: 119,659,558-119,661,357 , GRCh37.p13 chr2: 120,417,134-120,418,933 CFAP221
    nsv5584470copy number variation1nstd207human GRCh38 chr2: 119,552,287-119,552,414 , GRCh37.p13 chr2: 120,309,863-120,309,990 CFAP221
    nsv5565918copy number variation1nstd207human GRCh38 chr2: 119,552,753-119,552,808 , GRCh37.p13 chr2: 120,310,329-120,310,384 CFAP221
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449651copy number variation1nstd206human GRCh38 chr2: 119,659,483-119,660,932 , GRCh37.p13 chr2: 120,417,059-120,418,508 CFAP221
    nsv5380607translocation1nstd200human GRCh38 chr2: 119,660,919-119,660,919 , GRCh38 chr2: 119,660,258-119,660,258 , GRCh37.p13 chr2: 120,417,834-120,417,834 , GRCh37.p13 chr2: 120,418,495-120,418,495 CFAP221
    nsv5366480translocation1nstd200human GRCh38 chr2: 119,659,503-119,659,503 , GRCh38 chr2: 119,660,919-119,660,919 , GRCh37.p13 chr2: 120,418,495-120,418,495 , GRCh37.p13 chr2: 120,417,079-120,417,079 CFAP221
    nsv5361069translocation1nstd200human GRCh38 chr2: 119,659,624-119,659,624 , GRCh38 chr2: 119,660,919-119,660,919 , GRCh37.p13 chr2: 120,417,200-120,417,200 , GRCh37.p13 chr2: 120,418,495-120,418,495 CFAP221
    nsv5338546translocation1nstd200human GRCh37 chr2: 120,417,079-120,417,079 , GRCh37 chr2: 120,418,495-120,418,495 , GRCh38.p12 chr2: 119,660,919-119,660,919 , GRCh38.p12 chr2: 119,659,503-119,659,503 CFAP221
    nsv5337363translocation1nstd200human GRCh37 chr2: 120,418,495-120,418,495 , GRCh37 chr2: 120,417,200-120,417,200 , GRCh38.p12 chr2: 119,659,624-119,659,624 , GRCh38.p12 chr2: 119,660,919-119,660,919 CFAP221
    nsv5329498translocation1nstd204human GRCh38.p13 chr2: 119,659,503-119,659,503 , GRCh38.p13 chr2: 119,660,919-119,660,919 , GRCh37.p13 chr2: 120,417,079-120,417,079 , GRCh37.p13 chr2: 120,418,495-120,418,495 CFAP221
    nsv5322422translocation1nstd204human GRCh38.p13 chr2: 119,659,624-119,659,624 , GRCh38.p13 chr2: 119,660,919-119,660,919 , GRCh37.p13 chr2: 120,418,495-120,418,495 , GRCh37.p13 chr2: 120,417,200-120,417,200 CFAP221
    nsv5292777copy number variation1nstd204human GRCh37.p13 chr2: 120,101,316-120,449,316 , GRCh38.p13 chr2: 119,343,740-119,691,740 DBI, SCTR, 5 more genes
    nsv5216625copy number variation1nstd204human GRCh38.p13 chr2: 119,629,428-119,666,775 , GRCh37.p13 chr2: 120,387,004-120,424,351 CFAP221
    nsv5214356copy number variation1nstd204human GRCh38.p13 chr2: 119,604,702-119,605,901 , GRCh37.p13 chr2: 120,362,278-120,363,477 CFAP221
    nsv5214305copy number variation1nstd204human GRCh38.p13 chr2: 119,534,411-119,570,743 , GRCh37.p13 chr2: 120,291,987-120,328,319 CFAP221
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