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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965659insertion1nstd209human GRCh38 chr2: 207,865,802-207,865,802 , GRCh37.p13 chr2: 208,730,526-208,730,526 PLEKHM3
    nsv5952560insertion1nstd209human GRCh38 chr2: 208,024,142-208,024,142 , GRCh37.p13 chr2: 208,888,866-208,888,866 PLEKHM3
    nsv5905867copy number variation1nstd209human GRCh38 chr2: 207,842,186-207,844,557 , GRCh37.p13 chr2: 208,706,910-208,709,281 PLEKHM3
    nsv5899846copy number variation1nstd209human GRCh38 chr2: 207,820,854-207,820,904 , GRCh37.p13 chr2: 208,685,578-208,685,628 PLEKHM3
    nsv5832699copy number variation1nstd209human GRCh38 chr2: 207,842,167-207,844,531 , GRCh37.p13 chr2: 208,706,891-208,709,255 PLEKHM3
    nsv5719863mobile element insertion1nstd211human GRCh38 chr2: 207,950,161-207,950,161 , GRCh37.p13 chr2: 208,814,885-208,814,885 PLEKHM3
    nsv5719361mobile element insertion1nstd211human GRCh38 chr2: 207,931,323-207,931,323 , GRCh37.p13 chr2: 208,796,047-208,796,047 PLEKHM3
    nsv5692525mobile element insertion1nstd211human GRCh38 chr2: 207,841,481-207,841,481 , GRCh37.p13 chr2: 208,706,205-208,706,205 PLEKHM3
    nsv5688597mobile element insertion2nstd211human GRCh38 chr2: 207,889,454-207,889,454 , GRCh37.p13 chr2: 208,754,178-208,754,178 PLEKHM3
    nsv5686952mobile element insertion1nstd211human GRCh38 chr2: 207,857,743-207,857,743 , GRCh37.p13 chr2: 208,722,467-208,722,467 PLEKHM3
    nsv5681045mobile element insertion2nstd211human GRCh38 chr2: 208,023,324-208,023,324 , GRCh37.p13 chr2: 208,888,048-208,888,048 PLEKHM3
    nsv5678710mobile element insertion1nstd211human GRCh38 chr2: 208,008,525-208,008,525 , GRCh37.p13 chr2: 208,873,249-208,873,249 PLEKHM3
    nsv5677629mobile element insertion1nstd211human GRCh38 chr2: 207,959,118-207,959,118 , GRCh37.p13 chr2: 208,823,842-208,823,842 PLEKHM3
    nsv5619529insertion1nstd207human GRCh38 chr2: 208,023,306-208,023,306 , GRCh37.p13 chr2: 208,888,030-208,888,030 PLEKHM3
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5558354mobile element insertion1nstd206human GRCh38 chr2: 207,931,323-207,931,374 , GRCh37.p13 chr2: 208,796,047-208,796,098 PLEKHM3
    nsv5549235insertion1nstd206human GRCh38 chr2: 207,830,710-207,830,715 , GRCh37.p13 chr2: 208,695,434-208,695,439 PLEKHM3
    nsv5445747copy number variation1nstd206human GRCh38 chr2: 207,842,228-207,844,552 , GRCh37.p13 chr2: 208,706,952-208,709,276 PLEKHM3
    nsv5438471copy number variation1nstd206human GRCh38 chr2: 207,989,009-207,989,552 , GRCh37.p13 chr2: 208,853,733-208,854,276 PLEKHM3
    nsv5437757copy number variation1nstd206human GRCh38 chr2: 207,851,615-207,853,303 , GRCh37.p13 chr2: 208,716,339-208,718,027 PLEKHM3
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