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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946817copy number variation1nstd209human GRCh38 chr13: 68,839,720-68,871,684 , GRCh37.p13 chr13: 69,413,852-69,445,816 LINC00550, LOC105370254
    nsv5928778copy number variation1nstd209human GRCh38 chr13: 68,864,576-68,917,868 , GRCh37.p13 chr13: 69,438,708-69,492,000 LINC00550, LINC02342, 1 more genes
    nsv5867068copy number variation2nstd209human GRCh38 chr13: 68,879,351-68,880,550 , GRCh37.p13 chr13: 69,453,483-69,454,682 LINC02342, LINC00550
    nsv5859451copy number variation2nstd209human GRCh38 chr13: 68,863,239-68,873,432 , GRCh37.p13 chr13: 69,437,371-69,447,564 LOC105370254, LINC00550
    nsv5857048copy number variation2nstd209human GRCh38 chr13: 68,876,151-68,878,750 , GRCh37.p13 chr13: 69,450,283-69,452,882 LINC00550, LINC02342
    nsv5854779copy number variation1nstd209human GRCh38 chr13: 68,861,939-68,865,688 , GRCh37.p13 chr13: 69,436,071-69,439,820 LINC00550
    nsv5853537copy number variation1nstd209human GRCh38 chr13: 68,865,889-68,905,360 , GRCh37.p13 chr13: 69,440,021-69,479,492 LOC105370254, LINC00550, 1 more genes
    nsv5699740mobile element insertion1nstd211human GRCh38 chr13: 68,871,502-68,871,502 , GRCh37.p13 chr13: 69,445,634-69,445,634 LINC00550, LOC105370254
    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
    nsv5498909copy number variation1nstd206human GRCh38 chr13: 68,876,898-68,891,439 , GRCh37.p13 chr13: 69,451,030-69,465,571 LINC00550, LINC02342
    nsv5498522copy number variation1nstd206human GRCh38 chr13: 68,872,632-68,875,798 , GRCh37.p13 chr13: 69,446,764-69,449,930 LINC00550, LOC105370254
    nsv5497242copy number variation1nstd206human GRCh38 chr13: 68,877,955-68,878,201 , GRCh37.p13 chr13: 69,452,087-69,452,333 LINC02342, LINC00550
    nsv5348667translocation1nstd200human GRCh38 chr13: 68,891,439-68,891,439 , GRCh38 chr13: 68,876,896-68,876,896 , GRCh37.p13 chr13: 69,451,028-69,451,028 , GRCh37.p13 chr13: 69,465,571-69,465,571 LINC02342, LINC00550
    nsv5307600copy number variation1nstd204human GRCh38.p13 chr13: 67,378,459-71,217,205 , GRCh37.p13 chr13: 67,952,591-71,791,337 SRSF1P1, RN7SL761P, 32 more genes
    nsv5279557copy number variation1nstd204human GRCh38.p13 chr13: 68,864,539-68,900,899 , GRCh37.p13 chr13: 69,438,671-69,475,031 LINC02342, LINC00550, 1 more genes
    nsv5278295copy number variation1nstd204human GRCh38.p13 chr13: 68,878,201-68,884,200 , GRCh37.p13 chr13: 69,452,333-69,458,332 LINC00550, LINC02342
    nsv5276914copy number variation1nstd204human GRCh38.p13 chr13: 68,872,433-68,875,365 , GRCh37.p13 chr13: 69,446,565-69,449,497 LINC00550, LOC105370254
    nsv5271286copy number variation1nstd204human GRCh38.p13 chr13: 68,860,701-68,863,600 , GRCh37.p13 chr13: 69,434,833-69,437,732 LINC00550
    nsv5264546copy number variation1nstd204human GRCh38.p13 chr13: 68,871,201-68,873,300 , GRCh37.p13 chr13: 69,445,333-69,447,432 LOC105370254, LINC00550
    nsv5262331copy number variation1nstd204human GRCh38.p13 chr13: 68,872,601-68,875,600 , GRCh37.p13 chr13: 69,446,733-69,449,732 LINC00550, LOC105370254
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