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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv513984copy number variation453nstd46human NCBI36 chr1: 25,465,250-25,536,194 , GRCh38.p12 chr1: 25,266,172-25,337,116 , GRCh37.p13 chr1: 25,592,663-25,663,607 RHD, TMEM50A, 3 more genes
    nsv4401543copy number variation1nstd174human GRCh37 chr1: 25,558,560-25,673,142 , GRCh38.p12 chr1: 25,232,069-25,346,651 RHD, TMEM50A, 4 more genes

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