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Items: 1 to 20 of 335

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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
    nsv5887001copy number variation1nstd209human GRCh38 chr2: 66,621,755-66,623,974 , GRCh37.p13 chr2: 66,848,887-66,851,106 LINC01798
    nsv5874588copy number variation1nstd209human GRCh38 chr2: 66,626,192-66,626,702 , GRCh37.p13 chr2: 66,853,324-66,853,834 LINC01798
    nsv5874513copy number variation1nstd209human GRCh38 chr2: 66,665,989-66,673,152 , GRCh37.p13 chr2: 66,893,121-66,900,284 LINC01798
    nsv5874059copy number variation1nstd209human GRCh38 chr2: 66,660,993-66,661,422 , GRCh37.p13 chr2: 66,888,125-66,888,554 LINC01798
    nsv5833691copy number variation1nstd209human GRCh38 chr2: 66,666,248-66,673,179 , GRCh37.p13 chr2: 66,893,380-66,900,311 LINC01798
    nsv5833096copy number variation1nstd209human GRCh38 chr2: 66,671,930-66,672,929 , GRCh37.p13 chr2: 66,899,062-66,900,061 LINC01798
    nsv5685733mobile element insertion2nstd211human GRCh38 chr2: 66,631,389-66,631,389 , GRCh37.p13 chr2: 66,858,521-66,858,521 LINC01798
    nsv5683215mobile element insertion2nstd211human GRCh38 chr2: 66,637,075-66,637,075 , GRCh37.p13 chr2: 66,864,207-66,864,207 LINC01798
    nsv5617411insertion1nstd207human GRCh38 chr2: 66,631,376-66,631,376 , GRCh37.p13 chr2: 66,858,508-66,858,508 LINC01798
    nsv5558813sequence alteration1nstd206human GRCh38 chr2: 66,621,757-66,621,764 , GRCh37.p13 chr2: 66,848,889-66,848,896 LINC01798
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5543120insertion1nstd206human GRCh38 chr2: 66,621,757-66,621,757 , GRCh37.p13 chr2: 66,848,889-66,848,889 LINC01798
    nsv5536285insertion1nstd206human GRCh38 chr2: 66,616,691-66,616,726 , GRCh37.p13 chr2: 66,843,823-66,843,858 LINC01798
    nsv5453650copy number variation1nstd206human GRCh38 chr2: 66,614,019-66,624,456 , GRCh37.p13 chr2: 66,841,151-66,851,588 LINC01798
    nsv5443109copy number variation1nstd206human GRCh38 chr2: 66,660,996-66,661,423 , GRCh37.p13 chr2: 66,888,128-66,888,555 LINC01798
    nsv5437954copy number variation1nstd206human GRCh38 chr2: 66,638,584-66,648,885 , GRCh37.p13 chr2: 66,865,716-66,876,017 LINC01798
    nsv5437921copy number variation1nstd206human GRCh38 chr2: 66,695,188-66,698,983 , GRCh37.p13 chr2: 66,922,320-66,926,115 LINC01798, LINC01797
    nsv5434245copy number variation1nstd206human GRCh38 chr2: 66,626,199-66,626,703 , GRCh37.p13 chr2: 66,853,331-66,853,835 LINC01798
    nsv5405441mobile element insertion1nstd206human GRCh38 chr2: 66,637,075-66,637,126 , GRCh37.p13 chr2: 66,864,207-66,864,258 LINC01798
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