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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122600copy number variation1nstd186human GRCh37 chr16: 67,821,897-67,824,920 , GRCh38.p12 chr16: 67,787,994-67,791,017 RANBP10
    nsv5980419copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,628,846-67,813,408 , GRCh38.p12 chr16: 67,594,943-67,779,505 CTCF, PARD6A, 6 more genes
    nsv5972362insertion1nstd209human GRCh38 chr16: 67,785,731-67,785,731 , GRCh37.p13 chr16: 67,819,634-67,819,634 RANBP10
    nsv5939707copy number variation1nstd209human GRCh38 chr16: 67,787,132-67,802,530 , GRCh37.p13 chr16: 67,821,035-67,836,433 RANBP10
    nsv5938017copy number variation1nstd209human GRCh38 chr16: 67,763,070-67,763,643 , GRCh37.p13 chr16: 67,796,973-67,797,546 RANBP10
    nsv5935846copy number variation1nstd209human GRCh38 chr16: 67,788,283-67,791,043 , GRCh37.p13 chr16: 67,822,186-67,824,946 RANBP10
    nsv5881625copy number variation1nstd209human GRCh38 chr16: 67,791,241-67,803,298 , GRCh37.p13 chr16: 67,825,144-67,837,201 RANBP10
    nsv5870734copy number variation1nstd209human GRCh38 chr16: 67,788,279-67,791,078 , GRCh37.p13 chr16: 67,822,182-67,824,981 RANBP10
    nsv5662369insertion3nstd207human GRCh38 chr16: 67,782,758-67,782,758 , GRCh37.p13 chr16: 67,816,661-67,816,661 RANBP10
    nsv5591730copy number variation1nstd207human GRCh38 chr16: 67,788,283-67,791,043 , GRCh37.p13 chr16: 67,822,186-67,824,946 RANBP10
    nsv5530856copy number variation1nstd206human GRCh38 chr16: 67,803,037-67,803,503 , GRCh37.p13 chr16: 67,836,940-67,837,406 RANBP10
    nsv5530002copy number variation1nstd206human GRCh38 chr16: 67,720,891-67,721,601 , GRCh37.p13 chr16: 67,754,794-67,755,504 RANBP10
    nsv5529323copy number variation1nstd206human GRCh38 chr16: 67,787,994-67,791,017 , GRCh37.p13 chr16: 67,821,897-67,824,920 RANBP10
    nsv5525265copy number variation1nstd206human GRCh38 chr16: 67,788,245-67,788,328 , GRCh37.p13 chr16: 67,822,148-67,822,231 RANBP10
    nsv5393187copy number variation1nstd186human GRCh37 chr16: 67,822,253-67,824,920 , GRCh38.p12 chr16: 67,788,350-67,791,017 RANBP10
    nsv5393128copy number variation1nstd186human GRCh37 chr16: 67,822,253-67,824,919 , GRCh38.p12 chr16: 67,788,350-67,791,016 RANBP10
    nsv5365683translocation1nstd200human GRCh38 chr16: 67,723,545-67,723,545 , GRCh38 chr16: 67,724,118-67,724,118 , GRCh37.p13 chr16: 67,757,448-67,757,448 , GRCh37.p13 chr16: 67,758,021-67,758,021 RANBP10
    nsv5333488translocation1nstd200human GRCh37 chr16: 67,757,448-67,757,448 , GRCh37 chr16: 67,758,021-67,758,021 , GRCh38.p12 chr16: 67,723,545-67,723,545 , GRCh38.p12 chr16: 67,724,118-67,724,118 RANBP10
    nsv5314654copy number variation1nstd204human GRCh38.p13 chr16: 67,788,314-67,791,046 , GRCh37.p13 chr16: 67,822,217-67,824,949 RANBP10
    nsv5279370copy number variation1nstd204human GRCh38.p13 chr16: 67,788,301-67,791,000 , GRCh37.p13 chr16: 67,822,204-67,824,903 RANBP10
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