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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315092insertion1nstd102humanUncertain significance GRCh38 chr4: 121,822,648-121,822,648 , GRCh37 chr4: 122,743,803-122,743,803 CCNA2, BBS7

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