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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890565copy number variation1nstd209human GRCh38 chr3: 141,062,834-141,062,991 , GRCh37.p13 chr3: 140,781,676-140,781,833 SPSB4
    nsv5690554mobile element insertion1nstd211human GRCh38 chr3: 141,106,149-141,106,149 , GRCh37.p13 chr3: 140,824,991-140,824,991 SPSB4
    nsv5439716copy number variation1nstd206human GRCh38 chr3: 141,062,836-141,062,992 , GRCh37.p13 chr3: 140,781,678-140,781,834 SPSB4
    nsv5436330copy number variation1nstd206human GRCh38 chr3: 141,058,122-141,059,835 , GRCh37.p13 chr3: 140,776,964-140,778,677 SPSB4
    nsv5407230mobile element insertion1nstd206human GRCh38 chr3: 141,106,149-141,106,200 , GRCh37.p13 chr3: 140,824,991-140,825,042 SPSB4
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5346592translocation1nstd200human GRCh38 chr3: 141,058,122-141,058,122 , GRCh38 chr3: 141,059,835-141,059,835 , GRCh37.p13 chr3: 140,776,964-140,776,964 , GRCh37.p13 chr3: 140,778,677-140,778,677 SPSB4
    nsv5319832copy number variation1nstd204human GRCh38.p13 chr3: 141,062,827-141,063,000 , GRCh37.p13 chr3: 140,781,669-140,781,842 SPSB4
    nsv5317253copy number variation1nstd204human GRCh38.p13 chr3: 141,095,935-141,100,408 , GRCh37.p13 chr3: 140,814,777-140,819,250 SPSB4
    nsv5230073copy number variation1nstd204human GRCh38.p13 chr3: 141,096,198-141,100,597 , GRCh37.p13 chr3: 140,815,040-140,819,439 SPSB4
    nsv5099450mobile element insertion1nstd203human GRCh38 chr3: 141,106,133-141,106,149 , GRCh37.p13 chr3: 140,824,975-140,824,991 SPSB4
    nsv5097235mobile element insertion1nstd203human GRCh38 chr3: 141,112,594-141,112,644 , GRCh37.p13 chr3: 140,831,436-140,831,486 SPSB4
    nsv5091589mobile element insertion1nstd203human GRCh38 chr3: 141,112,644-141,112,651 , GRCh37.p13 chr3: 140,831,486-140,831,493 SPSB4
    nsv5089936mobile element insertion1nstd203human GRCh38 chr3: 141,112,609-141,112,644 , GRCh37.p13 chr3: 140,831,451-140,831,486 SPSB4
    nsv5085818mobile element insertion1nstd203human GRCh38 chr3: 141,052,969-141,052,985 , GRCh37.p13 chr3: 140,771,811-140,771,827 SPSB4
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4928086copy number variation1nstd200human GRCh38 chr3: 141,146,816-141,146,948 , GRCh37.p13 chr3: 140,865,658-140,865,790 SPSB4
    nsv4928085copy number variation1nstd200human GRCh38 chr3: 141,144,339-141,147,698 , GRCh37.p13 chr3: 140,863,181-140,866,540 SPSB4
    nsv4928084copy number variation1nstd200human GRCh38 chr3: 141,118,655-141,122,524 , GRCh37.p13 chr3: 140,837,497-140,841,366 SPSB4
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