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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6954293copy number variation1nstd229human GRCh38 chr13: 53,665,601-53,843,500 , GRCh37.p13 chr13: 54,239,736-54,417,635 LINC00558
    nsv6953676copy number variation1nstd229human GRCh38 chr13: 53,644,001-53,839,500 , GRCh37.p13 chr13: 54,218,136-54,413,635 LINC00558
    nsv6951444copy number variation1nstd229human GRCh38 chr13: 53,846,298-53,846,499 , GRCh37.p13 chr13: 54,420,433-54,420,634 LINC00558
    nsv6948985copy number variation1nstd229human GRCh38 chr13: 53,824,695-53,837,428 , GRCh37.p13 chr13: 54,398,830-54,411,563 LINC00558
    nsv6948216copy number variation1nstd229human GRCh38 chr13: 53,864,326-53,910,072 , GRCh37.p13 chr13: 54,438,461-54,484,207 LINC00558
    nsv6947432copy number variation1nstd229human GRCh38 chr13: 53,857,652-53,859,605 , GRCh37.p13 chr13: 54,431,787-54,433,740 LINC00558
    nsv6944338copy number variation1nstd229human GRCh38 chr13: 53,828,112-53,836,310 , GRCh37.p13 chr13: 54,402,247-54,410,445 LINC00558
    nsv6943800copy number variation1nstd229human GRCh38 chr13: 53,876,617-53,958,801 , GRCh37.p13 chr13: 54,450,752-54,532,936 LINC00558
    nsv6941503copy number variation1nstd229human GRCh38 chr13: 53,823,390-55,127,279 , GRCh37.p13 chr13: 54,397,525-55,701,414 LINC00558, LOC105370213, 3 more genes
    nsv6940589copy number variation1nstd229human GRCh38 chr13: 53,665,001-53,897,900 , GRCh37.p13 chr13: 54,239,136-54,472,035 LINC00558
    nsv6940329copy number variation1nstd229human GRCh38 chr13: 53,843,214-53,847,905 , GRCh37.p13 chr13: 54,417,349-54,422,040 LINC00558
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6494457copy number variation1nstd223human GRCh38 chr13: 53,832,401-53,833,400 , GRCh37.p13 chr13: 54,406,536-54,407,535 LINC00558
    nsv6492168copy number variation1nstd223human GRCh38 chr13: 53,835,901-53,837,100 , GRCh37.p13 chr13: 54,410,036-54,411,235 LINC00558
    nsv6490715copy number variation1nstd223human GRCh38 chr13: 53,824,661-53,825,299 , GRCh37.p13 chr13: 54,398,796-54,399,434 LINC00558
    nsv6487735copy number variation1nstd223human GRCh38 chr13: 53,838,701-53,840,300 , GRCh37.p13 chr13: 54,412,836-54,414,435 LINC00558
    nsv6486292copy number variation1nstd223human GRCh38 chr13: 53,827,701-53,829,500 , GRCh37.p13 chr13: 54,401,836-54,403,635 LINC00558
    nsv6485716copy number variation1nstd223human GRCh38 chr13: 53,861,196-53,861,930 , GRCh37.p13 chr13: 54,435,331-54,436,065 LINC00558
    nsv6481167copy number variation1nstd223human GRCh38 chr13: 53,837,095-53,837,664 , GRCh37.p13 chr13: 54,411,230-54,411,799 LINC00558
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
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