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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7142486insertion1nstd232human GRCh37.p13 chr7: 155,493,638-155,493,638 , GRCh38.p12 chr7: 155,700,944-155,700,944 RBM33
    nsv7137106copy number variation1nstd102humanUncertain significance GRCh37 chr7: 154,633,174-155,446,847 , GRCh38.p12 chr7: 154,841,464-155,654,153 RBM33, RBM33-DT, 21 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv6837538copy number variation1nstd229human GRCh38 chr7: 155,729,767-155,732,266 , GRCh37.p13 chr7: 155,522,461-155,524,960 RBM33
    nsv6836855copy number variation1nstd229human GRCh38 chr7: 155,733,437-155,733,494 , GRCh37.p13 chr7: 155,526,131-155,526,188 RBM33
    nsv6835157copy number variation1nstd229human GRCh38 chr7: 155,586,961-156,721,504 , GRCh37.p13 chr7: 155,379,656-156,514,198 LOC105375597, RBM33, 15 more genes
    nsv6834022copy number variation1nstd229human GRCh38 chr7: 154,808,210-155,712,129 , GRCh37.p13 chr7: 154,599,920-155,504,823 RBM33, LOC105375594, 21 more genes
    nsv6832935copy number variation1nstd229human GRCh38 chr7: 155,654,083-155,658,684 , GRCh37.p13 chr7: 155,446,777-155,451,378 RBM33
    nsv6830956copy number variation1nstd229human GRCh38 chr7: 155,711,883-155,711,936 , GRCh37.p13 chr7: 155,504,577-155,504,630 RBM33
    nsv6827948copy number variation1nstd229human GRCh38 chr7: 155,723,501-155,728,200 , GRCh37.p13 chr7: 155,516,195-155,520,894 RBM33
    nsv6824525copy number variation1nstd229human GRCh38 chr7: 152,687,878-156,500,924 , GRCh37.p13 chr7: 152,384,963-156,293,618 RN7SKP280, LINC03010, 44 more genes
    nsv6823762copy number variation1nstd229human GRCh38 chr7: 155,649,101-155,658,000 , GRCh37.p13 chr7: 155,441,795-155,450,694 RBM33
    nsv6822561copy number variation1nstd229human GRCh38 chr7: 155,711,965-155,717,275 , GRCh37.p13 chr7: 155,504,659-155,509,969 RBM33
    nsv6822123copy number variation1nstd229human GRCh38 chr7: 155,632,906-155,644,281 , GRCh37.p13 chr7: 155,425,600-155,436,975 RBM33-DT, RBM33
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6566734inversion1nstd223human GRCh38 chr7: 155,677,400-155,678,973 , GRCh37.p13 chr7: 155,470,094-155,471,667 RBM33
    nsv6434611copy number variation1nstd223human GRCh38 chr7: 155,699,460-155,700,249 , GRCh37.p13 chr7: 155,492,154-155,492,943 RBM33
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