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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7032449copy number variation1nstd229human GRCh38 chr20: 35,708,153-35,708,613 , GRCh37.p13 chr20: 34,296,075-34,296,535 RBM39
    nsv7026354copy number variation1nstd229human GRCh38 chr20: 35,718,898-35,719,568 , GRCh37.p13 chr20: 34,306,820-34,307,490 RBM39
    nsv7021546copy number variation1nstd229human GRCh38 chr20: 35,670,601-35,703,300 , GRCh37.p13 chr20: 34,258,523-34,291,222 ROMO1, NFS1, 1 more genes
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7019999copy number variation1nstd229human GRCh38 chr20: 35,486,342-36,114,422 , GRCh37.p13 chr20: 34,074,168-34,702,344 HMGB3P2, NFS1, 24 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6599067inversion1nstd223human GRCh38 chr20: 35,736,691-35,737,327 , GRCh37.p13 chr20: 34,324,613-34,325,249 RBM39
    nsv6596277inversion1nstd223human GRCh38 chr20: 35,716,017-35,717,018 , GRCh37.p13 chr20: 34,303,939-34,304,940 RBM39
    nsv6532928copy number variation1nstd223human GRCh38 chr20: 35,722,276-35,724,260 , GRCh37.p13 chr20: 34,310,198-34,312,182 RBM39
    nsv6530018copy number variation1nstd223human GRCh38 chr20: 35,707,601-35,709,200 , GRCh37.p13 chr20: 34,295,523-34,297,122 RBM39
    nsv6526589copy number variation1nstd223human GRCh38 chr20: 35,709,091-35,709,643 , GRCh37.p13 chr20: 34,297,013-34,297,565 RBM39
    nsv6134023copy number variation1nstd213human GRCh37 chr20: 34,270,000-35,840,001 , GRCh38.p12 chr20: 35,682,078-37,211,598 RBL1, AAR2, 35 more genes
    nsv5970631insertion1nstd209human GRCh38 chr20: 35,722,414-35,722,414 , GRCh37.p13 chr20: 34,310,336-34,310,336 RBM39
    nsv5948413copy number variation1nstd209human GRCh38 chr20: 35,671,536-35,737,524 , GRCh37.p13 chr20: 34,259,458-34,325,446 NFS1, RBM39, 1 more genes
    nsv5882842copy number variation1nstd209human GRCh38 chr20: 35,724,289-35,725,288 , GRCh37.p13 chr20: 34,312,211-34,313,210 RBM39
    nsv5880867copy number variation1nstd209human GRCh38 chr20: 35,733,323-35,736,422 , GRCh37.p13 chr20: 34,321,245-34,324,344 RBM39
    nsv5879140copy number variation1nstd209human GRCh38 chr20: 35,716,337-35,737,159 , GRCh37.p13 chr20: 34,304,259-34,325,081 RBM39
    nsv5877016copy number variation1nstd209human GRCh38 chr20: 35,703,950-35,715,223 , GRCh37.p13 chr20: 34,291,872-34,303,145 RBM39
    nsv5876214copy number variation1nstd209human GRCh38 chr20: 35,713,662-35,716,961 , GRCh37.p13 chr20: 34,301,584-34,304,883 RBM39
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