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Items: 1 to 20 of 667

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956043insertion1nstd209human GRCh38 chr5: 129,701,764-129,701,764 , GRCh37.p13 chr5: 129,037,457-129,037,457 ADAMTS19
    nsv5952974insertion1nstd209human GRCh38 chr5: 129,471,450-129,471,450 , GRCh37.p13 chr5: 128,807,143-128,807,143 ADAMTS19
    nsv5904164copy number variation1nstd209human GRCh38 chr5: 129,684,683-129,688,501 , GRCh37.p13 chr5: 129,020,376-129,024,194 ADAMTS19
    nsv5897339copy number variation1nstd209human GRCh38 chr5: 129,545,586-129,548,316 , GRCh37.p13 chr5: 128,881,279-128,884,009 ADAMTS19
    nsv5896111copy number variation1nstd209human GRCh38 chr5: 129,531,666-129,531,794 , GRCh37.p13 chr5: 128,867,359-128,867,487 ADAMTS19
    nsv5841741copy number variation1nstd209human GRCh38 chr5: 129,545,604-129,548,424 , GRCh37.p13 chr5: 128,881,297-128,884,117 ADAMTS19
    nsv5841740copy number variation1nstd209human GRCh38 chr5: 129,536,649-129,545,403 , GRCh37.p13 chr5: 128,872,342-128,881,096 ADAMTS19
    nsv5841645copy number variation1nstd209human GRCh38 chr5: 129,684,654-129,688,453 , GRCh37.p13 chr5: 129,020,347-129,024,146 ADAMTS19
    nsv5841092copy number variation1nstd209human GRCh38 chr5: 129,685,254-129,686,653 , GRCh37.p13 chr5: 129,020,947-129,022,346 ADAMTS19
    nsv5691202mobile element insertion2nstd211human GRCh38 chr5: 129,514,131-129,514,131 , GRCh37.p13 chr5: 128,849,824-128,849,824 ADAMTS19
    nsv5690097mobile element insertion1nstd211human GRCh38 chr5: 129,604,568-129,604,568 , GRCh37.p13 chr5: 128,940,261-128,940,261 ADAMTS19
    nsv5680898mobile element insertion1nstd211human GRCh38 chr5: 129,548,821-129,548,821 , GRCh37.p13 chr5: 128,884,514-128,884,514 ADAMTS19
    nsv5674339mobile element insertion2nstd211human GRCh38 chr5: 129,568,353-129,568,353 , GRCh37.p13 chr5: 128,904,046-128,904,046 ADAMTS19
    nsv5640754insertion2nstd207human GRCh38 chr5: 129,549,914-129,549,914 , GRCh37.p13 chr5: 128,885,607-128,885,607 ADAMTS19
    nsv5637102insertion1nstd207human GRCh38 chr5: 129,578,374-129,578,374 , GRCh37.p13 chr5: 128,914,067-128,914,067 ADAMTS19
    nsv5632246insertion2nstd207human GRCh38 chr5: 129,578,103-129,578,103 , GRCh37.p13 chr5: 128,913,796-128,913,796 ADAMTS19
    nsv5580872copy number variation1nstd207human GRCh38 chr5: 129,549,796-129,549,879 , GRCh37.p13 chr5: 128,885,489-128,885,572 ADAMTS19
    nsv5574946copy number variation1nstd207human GRCh38 chr5: 129,549,845-129,550,030 , GRCh37.p13 chr5: 128,885,538-128,885,723 ADAMTS19
    nsv5565957copy number variation1nstd207human GRCh38 chr5: 129,545,578-129,548,368 , GRCh37.p13 chr5: 128,881,271-128,884,061 ADAMTS19
    nsv5564989copy number variation1nstd207human GRCh38 chr5: 129,578,103-129,578,174 , GRCh37.p13 chr5: 128,913,796-128,913,867 ADAMTS19
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