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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv23722sequence alteration1estd20human NCBI36 chr7: 113,514,125-113,515,838 , GRCh37.p13 chr7: 113,726,889-113,728,602 , GRCh38.p12 chr7: 114,086,834-114,088,547 FOXP2

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