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Items: 1 to 20 of 366

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974385inversion1nstd209human GRCh38 chr2: 64,078,330-67,334,176 , GRCh37.p13 chr2: 64,305,464-67,561,308 , MEIS1, 63 more genes
    nsv5958084insertion1nstd209human GRCh38 chr2: 64,641,014-64,641,014 , GRCh37.p13 chr2: 64,868,148-64,868,148 SERTAD2
    nsv5833999copy number variation1nstd209human GRCh38 chr2: 64,715,843-64,716,842 , GRCh37.p13 chr2: 64,942,977-64,943,976 SERTAD2
    nsv5725633mobile element insertion1nstd211human GRCh38 chr2: 64,720,558-64,720,558 , GRCh37.p13 chr2: 64,947,692-64,947,692 SERTAD2
    nsv5679294mobile element insertion2nstd211human GRCh38 chr2: 64,698,913-64,698,913 , GRCh37.p13 chr2: 64,926,047-64,926,047 SERTAD2
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453734copy number variation1nstd206human GRCh38 chr2: 64,725,547-64,725,606 , GRCh37.p13 chr2: 64,952,681-64,952,740 SERTAD2
    nsv5439991copy number variation1nstd206human GRCh38 chr2: 64,692,690-64,695,485 , GRCh37.p13 chr2: 64,919,824-64,922,619 SERTAD2
    nsv5439610copy number variation1nstd206human GRCh38 chr2: 64,725,196-64,725,757 , GRCh37.p13 chr2: 64,952,330-64,952,891 SERTAD2
    nsv5406161mobile element insertion1nstd206human GRCh38 chr2: 64,698,913-64,698,964 , GRCh37.p13 chr2: 64,926,047-64,926,098 SERTAD2
    nsv5360713translocation1nstd200human GRCh38 chr2: 64,650,332-64,650,332 , GRCh38 chr2: 64,650,800-64,650,800 , GRCh37.p13 chr2: 64,877,466-64,877,466 , GRCh37.p13 chr2: 64,877,934-64,877,934 SERTAD2
    nsv5332326translocation1nstd200human GRCh37 chr2: 64,877,934-64,877,934 , GRCh37 chr2: 64,877,466-64,877,466 , GRCh38.p12 chr2: 64,650,332-64,650,332 , GRCh38.p12 chr2: 64,650,800-64,650,800 SERTAD2
    nsv5320732translocation1nstd204human GRCh38.p13 chr2: 64,650,332-64,650,332 , GRCh38.p13 chr2: 64,650,800-64,650,800 , GRCh37.p13 chr2: 64,877,934-64,877,934 , GRCh37.p13 chr2: 64,877,466-64,877,466 SERTAD2
    nsv5288311copy number variation1nstd204human GRCh38.p13 chr2: 64,653,481-64,653,938 , GRCh37.p13 chr2: 64,880,615-64,881,072 SERTAD2
    nsv5187437mobile element insertion1nstd203human GRCh38 chr2: 64,690,124-64,690,138 , GRCh37.p13 chr2: 64,917,258-64,917,272 SERTAD2
    nsv5077948mobile element insertion1nstd203human GRCh38 chr2: 64,670,131-64,670,145 , GRCh37.p13 chr2: 64,897,265-64,897,279 SERTAD2
    nsv4908759copy number variation1nstd200human GRCh38 chr2: 64,693,014-64,695,242 , GRCh37.p13 chr2: 64,920,148-64,922,376 SERTAD2
    nsv4908758copy number variation1nstd200human GRCh38 chr2: 64,685,842-64,843,970 , GRCh37.p13 chr2: 64,912,976-65,071,104 RN7SL341P, LOC105374776, 2 more genes
    nsv4901610copy number variation1nstd200human GRCh38 chr2: 64,712,969-64,714,541 , GRCh37.p13 chr2: 64,940,103-64,941,675 SERTAD2
    nsv4770468copy number variation1nstd200human GRCh37 chr2: 64,880,624-64,881,064 , GRCh38.p12 chr2: 64,653,490-64,653,930 SERTAD2
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