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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4399498copy number variation1nstd174human GRCh37 chr1: 16,185,814-16,193,131 , GRCh38.p12 chr1: 15,859,319-15,866,636 SPEN
    nsv829559copy number variation3nstd67human NCBI36 chr1: 16,058,573-16,065,542 , GRCh37.p13 chr1: 16,185,986-16,192,955 , GRCh38.p12 chr1: 15,859,491-15,866,460 SPEN

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