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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4410589copy number variation1nstd174human GRCh37 chr3: 191,011,204-191,013,666 , GRCh38.p12 chr3: 191,293,415-191,295,877 UTS2B
    esv3599101copy number variation45estd214human GRCh37 chr3: 191,011,204-191,013,667 , GRCh38.p12 chr3: 191,293,415-191,295,878 UTS2B

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