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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131372insertion1nstd186human GRCh37 chr19: 8,313,785-8,313,788 , GRCh38.p12 chr19: 8,248,901-8,248,904 CERS4
    nsv5974277insertion1nstd209human GRCh38 chr19: 8,248,871-8,248,871 , GRCh37.p13 chr19: 8,313,755-8,313,755 CERS4
    nsv5946278copy number variation1nstd209human GRCh38 chr19: 8,249,150-8,249,203 , GRCh37.p13 chr19: 8,314,034-8,314,087 CERS4
    nsv5945326copy number variation1nstd209human GRCh38 chr19: 8,231,588-8,231,883 , GRCh37.p13 chr19: 8,296,472-8,296,767 CERS4
    nsv5941176copy number variation1nstd209human GRCh38 chr19: 8,236,982-8,237,829 , GRCh37.p13 chr19: 8,301,866-8,302,713 CERS4, LOC107985282
    nsv5939845copy number variation1nstd209human GRCh38 chr19: 8,234,598-8,234,653 , GRCh37.p13 chr19: 8,299,482-8,299,537 CERS4
    nsv5935526copy number variation1nstd209human GRCh38 chr19: 8,221,608-8,222,560 , GRCh37.p13 chr19: 8,286,492-8,287,444 CERS4
    nsv5717501mobile element insertion2nstd211human GRCh38 chr19: 8,247,751-8,247,751 , GRCh37.p13 chr19: 8,312,635-8,312,635 CERS4
    nsv5653545insertion1nstd207human GRCh38 chr19: 8,247,735-8,247,735 , GRCh37.p13 chr19: 8,312,619-8,312,619 CERS4
    nsv5653303insertion1nstd207human GRCh38 chr19: 8,248,871-8,248,871 , GRCh37.p13 chr19: 8,313,755-8,313,755 CERS4
    nsv5535512insertion1nstd206human GRCh38 chr19: 8,248,901-8,248,904 , GRCh37.p13 chr19: 8,313,785-8,313,788 CERS4
    nsv5521941copy number variation1nstd206human GRCh38 chr19: 8,219,155-8,237,744 , GRCh37.p13 chr19: 8,284,039-8,302,628 CERS4
    nsv5521905copy number variation1nstd206human GRCh38 chr19: 8,234,601-8,234,654 , GRCh37.p13 chr19: 8,299,485-8,299,538 CERS4
    nsv5521656copy number variation1nstd206human GRCh38 chr19: 8,236,270-8,236,326 , GRCh37.p13 chr19: 8,301,154-8,301,210 CERS4
    nsv5520320copy number variation1nstd206human GRCh38 chr19: 8,211,579-8,216,553 , GRCh37.p13 chr19: 8,276,463-8,281,437 CERS4
    nsv5518486copy number variation1nstd206human GRCh38 chr19: 8,248,624-8,249,031 , GRCh37.p13 chr19: 8,313,508-8,313,915 CERS4
    nsv5515621copy number variation1nstd206human GRCh38 chr19: 8,248,490-8,248,551 , GRCh37.p13 chr19: 8,313,374-8,313,435 CERS4
    nsv5514389copy number variation1nstd206human GRCh38 chr19: 8,222,136-8,222,460 , GRCh37.p13 chr19: 8,287,020-8,287,344 CERS4
    nsv5365838translocation1nstd200human GRCh38 chr19: 8,261,289-8,261,289 , GRCh38 chr20: 35,815,836-35,815,836 , GRCh37.p13 chr19: 8,326,173-8,326,173 , GRCh37.p13 chr20: 34,403,758-34,403,758 PHF20, CERS4
    nsv5342562translocation1nstd200human GRCh37 chr19: 8,326,173-8,326,173 , GRCh37 chr20: 34,403,758-34,403,758 , GRCh38.p12 chr20: 35,815,836-35,815,836 , GRCh38.p12 chr19: 8,261,289-8,261,289 PHF20, CERS4
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