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Items: 1 to 20 of 467

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887219copy number variation1nstd209human GRCh38 chr2: 43,660,421-43,666,499 , GRCh37.p13 chr2: 43,887,560-43,893,638 PLEKHH2
    nsv5886852copy number variation1nstd209human GRCh38 chr2: 43,549,190-43,675,530 , GRCh37.p13 chr2: 43,776,329-43,902,669 THADA, PLEKHH2, 1 more genes
    nsv5884564copy number variation1nstd209human GRCh38 chr2: 43,656,891-43,656,969 , GRCh37.p13 chr2: 43,884,030-43,884,108 PLEKHH2
    nsv5882069copy number variation1nstd209human GRCh38 chr2: 43,645,572-43,645,822 , GRCh37.p13 chr2: 43,872,711-43,872,961 PLEKHH2
    nsv5833566copy number variation1nstd209human GRCh38 chr2: 43,666,056-43,675,544 , GRCh37.p13 chr2: 43,893,195-43,902,683 PLEKHH2, C1GALT1C1L
    nsv5833344copy number variation1nstd209human GRCh38 chr2: 43,760,076-43,769,010 , GRCh37.p13 chr2: 43,987,215-43,996,149 PLEKHH2
    nsv5833250copy number variation1nstd209human GRCh38 chr2: 43,670,795-43,671,894 , GRCh37.p13 chr2: 43,897,934-43,899,033 PLEKHH2
    nsv5722234mobile element insertion1nstd211human GRCh38 chr2: 43,758,270-43,758,270 , GRCh37.p13 chr2: 43,985,409-43,985,409 PLEKHH2
    nsv5622897insertion1nstd207human GRCh38 chr2: 43,754,167-43,754,167 , GRCh37.p13 chr2: 43,981,306-43,981,306 PLEKHH2
    nsv5584308copy number variation1nstd207human GRCh38 chr2: 43,660,421-43,666,499 , GRCh37.p13 chr2: 43,887,560-43,893,638 PLEKHH2
    nsv5583819copy number variation1nstd207human GRCh38 chr2: 43,677,904-43,677,953 , GRCh37.p13 chr2: 43,905,043-43,905,092 PLEKHH2
    nsv5452449copy number variation1nstd206human GRCh38 chr2: 43,754,161-43,754,333 , GRCh37.p13 chr2: 43,981,300-43,981,472 PLEKHH2
    nsv5451467copy number variation1nstd206human GRCh38 chr2: 43,726,957-43,727,035 , GRCh37.p13 chr2: 43,954,096-43,954,174 PLEKHH2
    nsv5444659copy number variation1nstd206human GRCh38 chr2: 43,660,417-43,666,520 , GRCh37.p13 chr2: 43,887,556-43,893,659 PLEKHH2
    nsv5439032copy number variation1nstd206human GRCh38 chr2: 43,654,427-43,786,469 , GRCh37.p13 chr2: 43,881,566-44,013,608 DYNC2LI1, PLEKHH2, 4 more genes
    nsv5393863mobile element deletion2nstd186human GRCh37 chr2: 43,887,576-43,893,639 , GRCh38.p12 chr2: 43,660,437-43,666,500 PLEKHH2
    nsv5375376translocation1nstd200human GRCh38 chr2: 43,639,211-43,639,211 , GRCh38 chr19: 35,567,077-35,567,077 , GRCh37.p13 chr19: 36,057,979-36,057,979 , GRCh37.p13 chr2: 43,866,350-43,866,350 PLEKHH2
    nsv5342952translocation1nstd200human GRCh37 chr2: 43,963,468-43,963,468 , GRCh37 chr2: 43,963,543-43,963,543 , GRCh38.p12 chr2: 43,736,329-43,736,329 , GRCh38.p12 chr2: 43,736,404-43,736,404 PLEKHH2
    nsv5331032translocation1nstd200human GRCh37 chr2: 43,902,670-43,902,670 , GRCh37 chr2: 43,776,329-43,776,329 , GRCh38.p12 chr2: 43,549,190-43,549,190 , GRCh38.p12 chr2: 43,675,531-43,675,531 THADA, PLEKHH2, 1 more genes
    nsv5324768mobile element deletion1nstd204human GRCh38.p13 chr2: 43,660,415-43,666,521 , GRCh37.p13 chr2: 43,887,554-43,893,660 PLEKHH2
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