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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1153012copy number variation1nstd107human GRCh37 (hg19) chr2: 24,453,460-24,465,012 , GRCh38 (hg38) chr2: 24,230,591-24,242,143 ITSN2

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