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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954234copy number variation1nstd209human GRCh38 chr20: 23,776,407-23,858,056 , GRCh37.p13 chr20: 23,757,044-23,838,693 CST2, LOC105372575, 2 more genes
    nsv5670285insertion1nstd207human GRCh38 chr20: 23,825,597-23,825,597 , GRCh37.p13 chr20: 23,806,234-23,806,234 CST2
    nsv5664545insertion1nstd207human GRCh38 chr20: 23,826,261-23,826,261 , GRCh37.p13 chr20: 23,806,898-23,806,898 CST2
    nsv5595441copy number variation1nstd207human GRCh38 chr20: 23,822,862-23,823,351 , GRCh37.p13 chr20: 23,803,499-23,803,988 CST2
    nsv5530305copy number variation1nstd206human GRCh38 chr20: 23,751,162-23,826,964 , GRCh37.p13 chr20: 23,731,799-23,807,601 CST2, LOC105372575, 3 more genes
    nsv5528895copy number variation1nstd206human GRCh38 chr20: 23,824,708-23,845,803 , GRCh37.p13 chr20: 23,805,345-23,826,440 CST2
    nsv5525647copy number variation1nstd206human GRCh38 chr20: 23,793,519-23,898,681 , GRCh37.p13 chr20: 23,774,156-23,879,318 LOC107985432, LOC105372575, 2 more genes
    nsv5522415copy number variation1nstd206human GRCh38 chr20: 23,822,766-23,822,828 , GRCh37.p13 chr20: 23,803,403-23,803,465 CST2
    nsv5520668copy number variation1nstd206human GRCh38 chr20: 23,766,481-23,847,827 , GRCh37.p13 chr20: 23,747,118-23,828,464 CST2, CSTP2, 2 more genes
    nsv5322621copy number variation1nstd204human GRCh38.p13 chr20: 23,750,862-23,827,307 , GRCh37.p13 chr20: 23,731,499-23,807,944 LOC105372575, CST2, 3 more genes
    nsv5299985copy number variation1nstd204human GRCh38.p13 chr20: 23,803,488-23,873,427 , GRCh37.p13 chr20: 23,784,125-23,854,064 CST2, LOC105372575, 1 more genes
    nsv5025218copy number variation1nstd200human GRCh38 chr20: 23,824,708-23,845,803 , GRCh37.p13 chr20: 23,805,345-23,826,440 CST2
    nsv5025217copy number variation1nstd200human GRCh38 chr20: 23,784,325-23,830,376 , GRCh37.p13 chr20: 23,764,962-23,811,013 LOC107985432, LOC105372575, 1 more genes
    nsv5025216copy number variation1nstd200human GRCh38 chr20: 23,751,111-23,827,066 , GRCh37.p13 chr20: 23,731,748-23,807,703 CST2, CSTP2, 3 more genes
    nsv5025213copy number variation1nstd200human GRCh38 chr20: 23,696,575-23,839,637 , GRCh37.p13 chr20: 23,677,212-23,820,274 CSTP2, CST2, 4 more genes
    nsv5021775copy number variation1nstd200human GRCh38 chr20: 23,823,856-23,826,877 , GRCh37.p13 chr20: 23,804,493-23,807,514 CST2
    nsv4865493copy number variation1nstd200human GRCh37 chr20: 23,805,345-23,826,440 , GRCh38.p12 chr20: 23,824,708-23,845,803 CST2
    nsv4865492copy number variation1nstd200human GRCh37 chr20: 23,731,745-23,807,698 , GRCh38.p12 chr20: 23,751,108-23,827,061 CST1, CSTP2, 3 more genes
    nsv4862369copy number variation1nstd200human GRCh37 chr20: 23,804,493-23,807,514 , GRCh38.p12 chr20: 23,823,856-23,826,877 CST2
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
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