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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv428403copy number variation13nstd8human GRCh38.p12 chr2: 129,818,076-130,882,067 , NCBI36 chr2: 130,292,119-131,356,110 , GRCh37.p13 chr2: 130,575,649-131,639,640 PTPN18, ARHGEF4, 60 more genes

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