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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927288copy number variation1nstd209human GRCh38 chr7: 2,377,767-2,378,293 , GRCh37.p13 chr7: 2,417,402-2,417,928 EIF3B
    nsv5912798copy number variation1nstd209human GRCh38 chr7: 2,361,846-2,362,028 , GRCh37.p13 chr7: 2,401,481-2,401,663 EIF3B
    nsv5911972copy number variation1nstd209human GRCh38 chr7: 2,377,465-2,377,784 , GRCh37.p13 chr7: 2,417,100-2,417,419 EIF3B
    nsv5909742copy number variation1nstd209human GRCh38 chr7: 2,377,580-2,378,260 , GRCh37.p13 chr7: 2,417,215-2,417,895 EIF3B
    nsv5683051mobile element insertion2nstd211human GRCh38 chr7: 2,359,055-2,359,055 , GRCh37.p13 chr7: 2,398,690-2,398,690 EIF3B
    nsv5643534insertion1nstd207human GRCh38 chr7: 2,378,122-2,378,122 , GRCh37.p13 chr7: 2,417,757-2,417,757 EIF3B
    nsv5643143insertion1nstd207human GRCh38 chr7: 2,377,693-2,377,693 , GRCh37.p13 chr7: 2,417,328-2,417,328 EIF3B
    nsv5642248insertion1nstd207human GRCh38 chr7: 2,377,749-2,377,749 , GRCh37.p13 chr7: 2,417,384-2,417,384 EIF3B
    nsv5640966insertion1nstd207human GRCh38 chr7: 2,378,012-2,378,012 , GRCh37.p13 chr7: 2,417,647-2,417,647 EIF3B
    nsv5640315insertion1nstd207human GRCh38 chr7: 2,377,509-2,377,509 , GRCh37.p13 chr7: 2,417,144-2,417,144 EIF3B
    nsv5639487insertion1nstd207human GRCh38 chr7: 2,377,618-2,377,618 , GRCh37.p13 chr7: 2,417,253-2,417,253 EIF3B
    nsv5636545insertion2nstd207human GRCh38 chr7: 2,377,913-2,377,913 , GRCh37.p13 chr7: 2,417,548-2,417,548 EIF3B
    nsv5632294insertion1nstd207human GRCh38 chr7: 2,377,531-2,377,531 , GRCh37.p13 chr7: 2,417,166-2,417,166 EIF3B
    nsv5631049insertion1nstd207human GRCh38 chr7: 2,378,076-2,378,076 , GRCh37.p13 chr7: 2,417,711-2,417,711 EIF3B
    nsv5625773insertion3nstd207human GRCh38 chr7: 2,378,317-2,378,317 , GRCh37.p13 chr7: 2,417,952-2,417,952 EIF3B
    nsv5580776copy number variation1nstd207human GRCh38 chr7: 2,377,548-2,377,739 , GRCh37.p13 chr7: 2,417,183-2,417,374 EIF3B
    nsv5573750copy number variation1nstd207human GRCh38 chr7: 2,377,631-2,378,075 , GRCh37.p13 chr7: 2,417,266-2,417,710 EIF3B
    nsv5572051copy number variation1nstd207human GRCh38 chr7: 2,378,315-2,378,376 , GRCh37.p13 chr7: 2,417,950-2,418,011 EIF3B
    nsv5571847copy number variation1nstd207human GRCh38 chr7: 2,378,120-2,378,368 , GRCh37.p13 chr7: 2,417,755-2,418,003 EIF3B
    nsv5568533copy number variation1nstd207human GRCh38 chr7: 2,377,467-2,377,530 , GRCh37.p13 chr7: 2,417,102-2,417,165 EIF3B
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