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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv508579copy number variation1nstd49human GRCh38.p12 chr10: 44,214,322-44,303,808 , NCBI35 chr10: 44,029,776-44,119,262 , GRCh37.p13 chr10: 44,709,770-44,799,256 CXCL12, LINC02881

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