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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5852223copy number variation1nstd209human GRCh38 chr13: 50,959,503-50,961,108 , GRCh37.p13 chr13: 51,533,639-51,535,244 RNASEH2B
    nsv5725068mobile element insertion1nstd211human GRCh38 chr13: 50,945,398-50,945,398 , GRCh37.p13 chr13: 51,519,534-51,519,534 RNASEH2B
    nsv5708523mobile element insertion2nstd211human GRCh38 chr13: 50,960,140-50,960,140 , GRCh37.p13 chr13: 51,534,276-51,534,276 RNASEH2B
    nsv5699375mobile element insertion1nstd211human GRCh38 chr13: 50,955,801-50,955,801 , GRCh37.p13 chr13: 51,529,937-51,529,937 RNASEH2B
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5559816mobile element insertion1nstd206human GRCh38 chr13: 50,945,398-50,945,449 , GRCh37.p13 chr13: 51,519,534-51,519,585 RNASEH2B
    nsv5513222copy number variation1nstd206human GRCh38 chr13: 50,921,702-50,921,775 , GRCh37.p13 chr13: 51,495,838-51,495,911 RNASEH2B
    nsv5510722copy number variation1nstd206human GRCh38 chr13: 50,938,800-50,941,776 , GRCh37.p13 chr13: 51,512,936-51,515,912 RNASEH2B
    nsv5503857copy number variation1nstd206human GRCh38 chr13: 50,942,547-50,942,610 , GRCh37.p13 chr13: 51,516,683-51,516,746 RNASEH2B
    nsv5430953mobile element insertion1nstd206human GRCh38 chr13: 50,955,801-50,955,852 , GRCh37.p13 chr13: 51,529,937-51,529,988 RNASEH2B
    nsv5430121mobile element insertion1nstd206human GRCh38 chr13: 50,960,140-50,960,191 , GRCh37.p13 chr13: 51,534,276-51,534,327 RNASEH2B
    nsv5307050copy number variation1nstd204human GRCh38.p13 chr13: 49,201,982-51,085,310 , GRCh37.p13 chr13: 49,776,118-51,659,446 , MLNR, 40 more genes
    nsv5268384copy number variation1nstd204human GRCh38.p13 chr13: 50,950,372-50,966,822 , GRCh37.p13 chr13: 51,524,508-51,540,958 RNASEH2B
    nsv5156023mobile element insertion1nstd203human GRCh38 chr13: 50,932,776-50,932,784 , GRCh37.p13 chr13: 51,506,912-51,506,920 RNASEH2B
    nsv5148022mobile element insertion1nstd203human GRCh38 chr13: 50,946,860-50,946,872 , GRCh37.p13 chr13: 51,520,996-51,521,008 RNASEH2B
    nsv5006472copy number variation1nstd200human GRCh38 chr13: 50,959,733-50,963,377 , GRCh37.p13 chr13: 51,533,869-51,537,513 RNASEH2B
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4845274copy number variation1nstd200human GRCh37 chr13: 49,776,128-51,659,444 , GRCh38.p12 chr13: 49,201,992-51,085,308 , PHF11, 40 more genes
    nsv4728809copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 45,487,628-52,639,336 , GRCh38.p12 chr13: 44,913,493-52,065,200 ATP7B, RCBTB2, 155 more genes
    nsv4678858copy number variation1nstd189human GRCh37.p13 chr13: 50,484,195-51,548,156 , GRCh38.p12 chr13: 49,910,059-50,974,020 , DLEU2, 17 more genes
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