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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946932copy number variation1nstd209human GRCh38 chr14: 21,250,884-21,252,709 , GRCh37.p13 chr14: 21,719,043-21,720,868 HNRNPC
    nsv5930941copy number variation1nstd209human GRCh38 chr14: 21,222,370-21,227,288 , GRCh37.p13 chr14: 21,690,529-21,695,447 HNRNPC
    nsv5929680copy number variation1nstd209human GRCh38 chr14: 21,251,197-21,251,281 , GRCh37.p13 chr14: 21,719,356-21,719,440 HNRNPC
    nsv5865518copy number variation1nstd209human GRCh38 chr14: 21,250,884-21,252,683 , GRCh37.p13 chr14: 21,719,043-21,720,842 HNRNPC
    nsv5864146copy number variation1nstd209human GRCh38 chr14: 21,222,390-21,226,289 , GRCh37.p13 chr14: 21,690,549-21,694,448 HNRNPC
    nsv5721746mobile element insertion1nstd211human GRCh38 chr14: 21,257,910-21,257,910 , GRCh37.p13 chr14: 21,726,069-21,726,069 HNRNPC
    nsv5701625mobile element insertion1nstd211human GRCh38 chr14: 21,243,775-21,243,775 , GRCh37.p13 chr14: 21,711,934-21,711,934 HNRNPC
    nsv5697869mobile element insertion1nstd211human GRCh38 chr14: 21,243,759-21,243,759 , GRCh37.p13 chr14: 21,711,918-21,711,918 HNRNPC
    nsv5663598insertion1nstd207human GRCh38 chr14: 21,260,117-21,260,117 , GRCh37.p13 chr14: 21,728,276-21,728,276 HNRNPC
    nsv5655240insertion1nstd207human GRCh38 chr14: 21,226,899-21,226,899 , GRCh37.p13 chr14: 21,695,058-21,695,058 HNRNPC
    nsv5561411mobile element insertion1nstd206human GRCh38 chr14: 21,257,860-21,257,896 , GRCh37.p13 chr14: 21,726,019-21,726,055 HNRNPC
    nsv5509495copy number variation1nstd206human GRCh38 chr14: 21,251,197-21,251,282 , GRCh37.p13 chr14: 21,719,356-21,719,441 HNRNPC
    nsv5508488copy number variation1nstd206human GRCh38 chr14: 21,222,372-21,227,289 , GRCh37.p13 chr14: 21,690,531-21,695,448 HNRNPC
    nsv5502320copy number variation1nstd206human GRCh38 chr14: 21,238,897-21,239,602 , GRCh37.p13 chr14: 21,707,056-21,707,761 HNRNPC
    nsv5500046copy number variation1nstd206human GRCh38 chr14: 21,243,262-21,243,312 , GRCh37.p13 chr14: 21,711,421-21,711,471 HNRNPC
    nsv5494084copy number variation1nstd206human GRCh38 chr14: 21,250,884-21,252,710 , GRCh37.p13 chr14: 21,719,043-21,720,869 HNRNPC
    nsv5415673mobile element insertion1nstd206human GRCh38 chr14: 21,243,775-21,243,810 , GRCh37.p13 chr14: 21,711,934-21,711,969 HNRNPC
    nsv5374431translocation1nstd200human GRCh38 chr14: 21,222,584-21,222,584 , GRCh38 chr14: 21,223,553-21,223,553 , GRCh37.p13 chr14: 21,691,712-21,691,712 , GRCh37.p13 chr14: 21,690,743-21,690,743 HNRNPC
    nsv5357024translocation1nstd200human GRCh38 chr14: 21,251,282-21,251,282 , GRCh38 chr14: 21,251,197-21,251,197 , GRCh37.p13 chr14: 21,719,356-21,719,356 , GRCh37.p13 chr14: 21,719,441-21,719,441 HNRNPC
    nsv5357023translocation1nstd200human GRCh38 chr14: 21,246,895-21,246,895 , GRCh38 chr14: 21,247,145-21,247,145 , GRCh37.p13 chr14: 21,715,054-21,715,054 , GRCh37.p13 chr14: 21,715,304-21,715,304 HNRNPC
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