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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv510412sequence alteration1nstd49human NCBI35 chr16: 11,273,653-11,279,653 , GRCh38.p12 chr16: 11,272,295-11,278,295 , GRCh37.p13 chr16: 11,366,152-11,372,152 PRM2, PRM3, 1 more genes

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