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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5900952copy number variation1nstd209human GRCh38 chr6: 15,549,741-15,551,811 , GRCh37.p13 chr6: 15,549,972-15,552,042 LOC105374947, DTNBP1
    nsv5898856copy number variation1nstd209human GRCh38 chr6: 15,534,604-15,534,677 , GRCh37.p13 chr6: 15,534,835-15,534,908 LOC105374947, DTNBP1
    nsv5844763copy number variation1nstd209human GRCh38 chr6: 15,549,694-15,551,693 , GRCh37.p13 chr6: 15,549,925-15,551,924 LOC105374947, DTNBP1
    nsv5564204copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr6: 15,523,206-16,146,982 , GRCh38.p12 chr6: 15,522,975-16,146,751 MDH1P2, LINC02543, 8 more genes
    nsv5473379copy number variation1nstd206human GRCh38 chr6: 15,660,867-15,661,014 , GRCh37.p13 chr6: 15,661,098-15,661,245 DTNBP1
    nsv5464828copy number variation1nstd206human GRCh38 chr6: 15,537,825-15,548,889 , GRCh37.p13 chr6: 15,538,056-15,549,120 DTNBP1, LOC105374947
    nsv5461179copy number variation1nstd206human GRCh38 chr6: 15,660,669-15,716,469 , GRCh37.p13 chr6: 15,660,900-15,716,700 LOC102724520, DTNBP1
    nsv5457221copy number variation1nstd206human GRCh38 chr6: 15,656,525-15,658,390 , GRCh37.p13 chr6: 15,656,756-15,658,621 DTNBP1
    nsv5378237translocation1nstd200human GRCh38 chr6: 15,660,264-15,660,264 , GRCh38 chr6: 15,660,188-15,660,188 , GRCh37.p13 chr6: 15,660,495-15,660,495 , GRCh37.p13 chr6: 15,660,419-15,660,419 DTNBP1
    nsv5378236translocation1nstd200human GRCh38 chr6: 15,656,525-15,656,525 , GRCh38 chr6: 15,658,390-15,658,390 , GRCh37.p13 chr6: 15,656,756-15,656,756 , GRCh37.p13 chr6: 15,658,621-15,658,621 DTNBP1
    nsv5369251translocation1nstd200human GRCh38 chr11: 59,754,201-59,754,201 , GRCh38 chr6: 15,654,726-15,654,726 , GRCh37.p13 chr6: 15,654,957-15,654,957 , GRCh37.p13 chr11: 59,521,674-59,521,674 DTNBP1, STX3
    nsv5369250translocation1nstd200human GRCh38 chr6: 15,608,203-15,608,203 , GRCh38 chr15: 69,452,822-69,452,822 , GRCh37.p13 chr6: 15,608,434-15,608,434 , GRCh37.p13 chr15: 69,745,161-69,745,161 DTNBP1, RPLP1
    nsv5341852translocation1nstd200human GRCh37 chr6: 15,654,957-15,654,957 , GRCh37 chr11: 59,521,674-59,521,674 , GRCh38.p12 chr11: 59,754,201-59,754,201 , GRCh38.p12 chr6: 15,654,726-15,654,726 STX3, DTNBP1
    nsv5307652copy number variation1nstd204human GRCh38.p13 chr6: 15,660,659-15,716,477 , GRCh37.p13 chr6: 15,660,890-15,716,708 LOC102724520, DTNBP1
    nsv5238121copy number variation1nstd204human GRCh38.p13 chr6: 15,660,828-15,666,462 , GRCh37.p13 chr6: 15,661,059-15,666,693 DTNBP1
    nsv5094700mobile element insertion1nstd203human GRCh38 chr6: 15,529,787-15,529,805 , GRCh37.p13 chr6: 15,530,018-15,530,036 LOC105374947, DTNBP1
    nsv5086315mobile element insertion1nstd203human GRCh38 chr6: 15,539,115-15,539,129 , GRCh37.p13 chr6: 15,539,346-15,539,360 LOC105374947, DTNBP1
    nsv4934451copy number variation1nstd200human GRCh38 chr6: 15,660,669-15,716,469 , GRCh37.p13 chr6: 15,660,900-15,716,700 LOC102724520, DTNBP1
    nsv4934450copy number variation1nstd200human GRCh38 chr6: 15,537,825-15,548,889 , GRCh37.p13 chr6: 15,538,056-15,549,120 DTNBP1, LOC105374947
    nsv4932850copy number variation1nstd200human GRCh38 chr6: 15,648,562-15,648,679 , GRCh37.p13 chr6: 15,648,793-15,648,910 DTNBP1
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