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Items: 1 to 20 of 555

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5946852copy number variation1nstd209human GRCh38 chr16: 18,904,365-18,904,666 , GRCh37.p13 chr16: 18,915,687-18,915,988 SMG1
    nsv5933931copy number variation1nstd209human GRCh38 chr16: 18,821,202-18,827,053 , GRCh37.p13 chr16: 18,832,524-18,838,375 SMG1
    nsv5932284copy number variation1nstd209human GRCh38 chr16: 18,911,564-18,917,729 , GRCh37.p13 chr16: 18,922,886-18,929,051 SMG1
    nsv5929687copy number variation1nstd209human GRCh38 chr16: 18,802,553-18,802,860 , GRCh37.p13 chr16: 18,813,875-18,814,182 SMG1
    nsv5868612copy number variation1nstd209human GRCh38 chr16: 18,912,282-18,917,907 , GRCh37.p13 chr16: 18,923,604-18,929,229 SMG1
    nsv5724485mobile element insertion2nstd211human GRCh38 chr16: 18,895,213-18,895,213 , GRCh37.p13 chr16: 18,906,535-18,906,535 SMG1
    nsv5717498mobile element insertion1nstd211human GRCh38 chr16: 18,909,047-18,909,047 , GRCh37.p13 chr16: 18,920,369-18,920,369 SMG1
    nsv5707876mobile element insertion1nstd211human GRCh38 chr16: 18,887,762-18,887,762 , GRCh37.p13 chr16: 18,899,084-18,899,084 SMG1
    nsv5694772mobile element insertion2nstd211human GRCh38 chr16: 18,894,697-18,894,697 , GRCh37.p13 chr16: 18,906,019-18,906,019 SMG1
    nsv5602072copy number variation1nstd207human GRCh38 chr16: 18,865,678-18,865,915 , GRCh37.p13 chr16: 18,877,000-18,877,237 SMG1
    nsv5597497copy number variation1nstd207human GRCh38 chr16: 18,867,701-18,868,002 , GRCh37.p13 chr16: 18,879,023-18,879,324 SMG1
    nsv5594994copy number variation1nstd207human GRCh38 chr16: 18,890,644-18,890,767 , GRCh37.p13 chr16: 18,901,966-18,902,089 SMG1
    nsv5593817copy number variation1nstd207human GRCh38 chr16: 18,916,228-18,916,543 , GRCh37.p13 chr16: 18,927,550-18,927,865 SMG1
    nsv5592260copy number variation1nstd207human GRCh38 chr16: 18,864,415-18,864,512 , GRCh37.p13 chr16: 18,875,737-18,875,834 SMG1
    nsv5590487copy number variation1nstd207human GRCh38 chr16: 18,856,094-18,856,329 , GRCh37.p13 chr16: 18,867,416-18,867,651 SMG1
    nsv5589884copy number variation1nstd207human GRCh38 chr16: 18,821,202-18,827,053 , GRCh37.p13 chr16: 18,832,524-18,838,375 SMG1
    nsv5587950copy number variation1nstd207human GRCh38 chr16: 18,888,702-18,889,058 , GRCh37.p13 chr16: 18,900,024-18,900,380 SMG1
    nsv5586001copy number variation1nstd207human GRCh38 chr16: 18,856,224-18,856,335 , GRCh37.p13 chr16: 18,867,546-18,867,657 SMG1
    nsv5585448copy number variation1nstd207human GRCh38 chr16: 18,864,460-18,864,683 , GRCh37.p13 chr16: 18,875,782-18,876,005 SMG1
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