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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4578236copy number variation1nstd180human GRCh37.p13 chrX: 114,141,331-114,141,411 , GRCh38 chrX: 114,906,768-114,906,848 , GRCh37.p13 chrX|NW_004070891.1: 575,570-575,650 HTR2C

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