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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974292insertion1nstd209human GRCh38 chr20: 51,848,593-51,848,593 , GRCh37.p13 chr20: 50,465,132-50,465,132 LINC01429
    nsv5966296copy number variation1nstd209human GRCh38 chr20: 51,839,750-51,845,927 , GRCh37.p13 chr20: 50,456,289-50,462,466 LINC01429
    nsv5961296copy number variation1nstd209human GRCh38 chr20: 51,835,580-51,844,116 , GRCh37.p13 chr20: 50,452,119-50,460,655 LINC01429
    nsv5959010copy number variation1nstd209human GRCh38 chr20: 51,833,024-51,846,396 , GRCh37.p13 chr20: 50,449,563-50,462,935 LINC01429
    nsv5951833copy number variation1nstd209human GRCh38 chr20: 51,844,087-51,844,221 , GRCh37.p13 chr20: 50,460,626-50,460,760 LINC01429
    nsv5878255copy number variation1nstd209human GRCh38 chr20: 51,833,683-51,843,898 , GRCh37.p13 chr20: 50,450,222-50,460,437 LINC01429
    nsv5874636copy number variation1nstd209human GRCh38 chr20: 51,837,284-51,845,298 , GRCh37.p13 chr20: 50,453,823-50,461,837 LINC01429
    nsv5868588copy number variation1nstd209human GRCh38 chr20: 51,841,399-51,843,398 , GRCh37.p13 chr20: 50,457,938-50,459,937 LINC01429
    nsv5714542mobile element insertion2nstd211human GRCh38 chr20: 51,852,919-51,852,919 , GRCh37.p13 chr20: 50,469,458-50,469,458 LINC01429
    nsv5710068mobile element insertion2nstd211human GRCh38 chr20: 51,848,610-51,848,610 , GRCh37.p13 chr20: 50,465,149-50,465,149 LINC01429
    nsv5561804mobile element insertion1nstd206human GRCh38 chr20: 51,852,919-51,852,970 , GRCh37.p13 chr20: 50,469,458-50,469,509 LINC01429
    nsv5549300insertion1nstd206human GRCh38 chr20: 51,854,908-51,854,910 , GRCh37.p13 chr20: 50,471,447-50,471,449 LINC01429
    nsv5526853copy number variation1nstd206human GRCh38 chr20: 51,855,464-51,856,248 , GRCh37.p13 chr20: 50,472,003-50,472,787 LINC01429
    nsv5521366copy number variation1nstd206human GRCh38 chr20: 51,840,547-51,847,199 , GRCh37.p13 chr20: 50,457,086-50,463,738 LINC01429
    nsv5350460translocation1nstd200human GRCh38 chr20: 51,854,910-51,854,910 , GRCh38 chr20: 51,854,305-51,854,305 , GRCh37.p13 chr20: 50,470,844-50,470,844 , GRCh37.p13 chr20: 50,471,449-50,471,449 LINC01429
    nsv5331469translocation1nstd200human GRCh37 chr20: 50,471,449-50,471,449 , GRCh37 chr20: 50,470,844-50,470,844 , GRCh38.p12 chr20: 51,854,305-51,854,305 , GRCh38.p12 chr20: 51,854,910-51,854,910 LINC01429
    nsv5281978copy number variation1nstd204human GRCh37.p13 chr20: 50,301,940-50,731,739 , GRCh38.p13 chr20: 51,685,401-52,115,200 ATP9A, ZFP64, 7 more genes
    nsv5176597mobile element insertion1nstd203human GRCh38 chr20: 51,848,593-51,848,610 , GRCh37.p13 chr20: 50,465,132-50,465,149 LINC01429
    nsv5169037mobile element insertion1nstd203human GRCh38 chr20: 51,829,892-51,829,920 , GRCh37.p13 chr20: 50,446,431-50,446,459 LINC01429
    nsv5025710copy number variation1nstd200human GRCh38 chr20: 51,861,166-51,978,813 , GRCh37.p13 chr20: 50,477,705-50,595,352 RNU6-347P, RNU7-6P, 1 more genes
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