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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4449727copy number variation1nstd178human GRCh37 chr16: 86,542,131-86,549,266 , GRCh38.p12 chr16: 86,508,525-86,515,660 FOXF1, FENDRR

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