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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904622copy number variation1nstd209human GRCh38 chr3: 146,515,504-146,520,756 , GRCh37.p13 chr3: 146,233,291-146,238,543 PLSCR1
    nsv5834702copy number variation1nstd209human GRCh38 chr3: 146,515,614-146,520,767 , GRCh37.p13 chr3: 146,233,401-146,238,554 PLSCR1
    nsv5692001mobile element insertion1nstd211human GRCh38 chr3: 146,540,497-146,540,497 , GRCh37.p13 chr3: 146,258,284-146,258,284 PLSCR1
    nsv5680658mobile element insertion1nstd211human GRCh38 chr3: 146,545,009-146,545,009 , GRCh37.p13 chr3: 146,262,796-146,262,796 PLSCR1
    nsv5411773mobile element insertion1nstd206human GRCh38 chr3: 146,545,009-146,545,060 , GRCh37.p13 chr3: 146,262,796-146,262,847 PLSCR1
    nsv5408388mobile element insertion1nstd206human GRCh38 chr3: 146,540,497-146,540,548 , GRCh37.p13 chr3: 146,258,284-146,258,335 PLSCR1
    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
    nsv5352006translocation1nstd200human GRCh38 chr3: 146,542,673-146,542,673 , GRCh38 chr3: 146,542,813-146,542,813 , GRCh37.p13 chr3: 146,260,460-146,260,460 , GRCh37.p13 chr3: 146,260,600-146,260,600 PLSCR1
    nsv5301803copy number variation1nstd204human GRCh38.p13 chr3: 145,088,231-147,513,312 , GRCh37.p13 chr3: 144,806,005-147,231,099 LINC02010, ZIC1, 21 more genes
    nsv5236950copy number variation1nstd204human GRCh38.p13 chr3: 146,492,428-146,519,842 , GRCh37.p13 chr3: 146,210,215-146,237,629 PLSCR1, PLSCR2
    nsv5235705copy number variation1nstd204human GRCh38.p13 chr3: 146,516,514-146,517,713 , GRCh37.p13 chr3: 146,234,301-146,235,500 PLSCR1
    nsv5232502copy number variation1nstd204human GRCh38.p13 chr3: 145,088,201-146,733,600 , GRCh37.p13 chr3: 144,805,975-146,451,387 PLSCR2, LOC105374143, 14 more genes
    nsv5231210copy number variation1nstd204human GRCh38.p13 chr3: 146,542,533-146,544,432 , GRCh37.p13 chr3: 146,260,320-146,262,219 PLSCR1
    nsv5084196mobile element insertion1nstd203human GRCh38 chr3: 146,525,795-146,525,811 , GRCh37.p13 chr3: 146,243,582-146,243,598 PLSCR1
    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
    nsv4924695copy number variation1nstd200human GRCh38 chr3: 146,485,150-146,513,435 , GRCh37.p13 chr3: 146,202,937-146,231,222 PLSCR1, PLSCR2
    nsv4914865copy number variation1nstd200human GRCh38 chr3: 145,886,271-146,782,511 , GRCh37.p13 chr3: 145,604,058-146,500,298 LOC105374145, PLSCR4P1, 8 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4804879copy number variation1nstd200human GRCh37 chr3: 146,202,937-146,231,222 , GRCh38.p12 chr3: 146,485,150-146,513,435 PLSCR1, PLSCR2
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