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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4416168copy number variation1nstd174human GRCh37 chr14: 99,637,645-99,642,792 , GRCh38.p12 chr14: 99,171,308-99,176,455 BCL11B
    esv2671501copy number variation76estd199human GRCh37 chr14: 99,637,645-99,642,792 , GRCh38.p12 chr14: 99,171,308-99,176,455 BCL11B

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