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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966165insertion1nstd209human GRCh38 chr7: 44,254,776-44,254,776 , GRCh37.p13 chr7: 44,294,375-44,294,375 CAMK2B
    nsv5927439copy number variation1nstd209human GRCh38 chr7: 44,227,036-44,227,127 , GRCh37.p13 chr7: 44,266,635-44,266,726 CAMK2B
    nsv5925136copy number variation1nstd209human GRCh38 chr7: 44,226,951-44,227,287 , GRCh37.p13 chr7: 44,266,550-44,266,886 CAMK2B
    nsv5921772copy number variation1nstd209human GRCh38 chr7: 44,277,739-44,277,796 , GRCh37.p13 chr7: 44,317,338-44,317,395 CAMK2B
    nsv5919540copy number variation1nstd209human GRCh38 chr7: 44,227,121-44,227,711 , GRCh37.p13 chr7: 44,266,720-44,267,310 CAMK2B
    nsv5916104copy number variation1nstd209human GRCh38 chr7: 44,227,422-44,227,774 , GRCh37.p13 chr7: 44,267,021-44,267,373 CAMK2B
    nsv5908017copy number variation1nstd209human GRCh38 chr7: 44,221,430-44,221,559 , GRCh37.p13 chr7: 44,261,029-44,261,158 CAMK2B
    nsv5677370mobile element insertion1nstd211human GRCh38 chr7: 44,285,993-44,285,993 , GRCh37.p13 chr7: 44,325,592-44,325,592 CAMK2B
    nsv5676434mobile element insertion2nstd211human GRCh38 chr7: 44,296,846-44,296,846 , GRCh37.p13 chr7: 44,336,445-44,336,445 CAMK2B
    nsv5643460insertion1nstd207human GRCh38 chr7: 44,254,776-44,254,776 , GRCh37.p13 chr7: 44,294,375-44,294,375 CAMK2B
    nsv5638666insertion1nstd207human GRCh38 chr7: 44,227,768-44,227,768 , GRCh37.p13 chr7: 44,267,367-44,267,367 CAMK2B
    nsv5625444insertion1nstd207human GRCh38 chr7: 44,227,766-44,227,766 , GRCh37.p13 chr7: 44,267,365-44,267,365 CAMK2B
    nsv5625376insertion1nstd207human GRCh38 chr7: 44,227,767-44,227,767 , GRCh37.p13 chr7: 44,267,366-44,267,366 CAMK2B
    nsv5582424copy number variation1nstd207human GRCh38 chr7: 44,227,051-44,227,403 , GRCh37.p13 chr7: 44,266,650-44,267,002 CAMK2B
    nsv5571491copy number variation1nstd207human GRCh38 chr7: 44,227,475-44,227,583 , GRCh37.p13 chr7: 44,267,074-44,267,182 CAMK2B
    nsv5570872copy number variation1nstd207human GRCh38 chr7: 44,227,049-44,227,104 , GRCh37.p13 chr7: 44,266,648-44,266,703 CAMK2B
    nsv5570237copy number variation1nstd207human GRCh38 chr7: 44,227,293-44,227,753 , GRCh37.p13 chr7: 44,266,892-44,267,352 CAMK2B
    nsv5568879copy number variation1nstd207human GRCh38 chr7: 44,227,062-44,227,174 , GRCh37.p13 chr7: 44,266,661-44,266,773 CAMK2B
    nsv5564727copy number variation1nstd207human GRCh38 chr7: 44,227,678-44,227,774 , GRCh37.p13 chr7: 44,267,277-44,267,373 CAMK2B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
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