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Items: 1 to 20 of 846

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964032insertion1nstd209human GRCh38 chr5: 80,803,524-80,803,524 , GRCh37.p13 chr5: 80,099,343-80,099,343 MSH3
    nsv5958128insertion1nstd209human GRCh38 chr5: 80,784,239-80,784,239 , GRCh37.p13 chr5: 80,080,058-80,080,058 MSH3
    nsv5906467copy number variation1nstd209human GRCh38 chr5: 80,842,262-80,843,213 , GRCh37.p13 chr5: 80,138,081-80,139,032 MSH3
    nsv5904091copy number variation1nstd209human GRCh38 chr5: 80,874,649-80,874,699 , GRCh37.p13 chr5: 80,170,468-80,170,518 MSH3
    nsv5903858copy number variation1nstd209human GRCh38 chr5: 80,851,301-80,851,465 , GRCh37.p13 chr5: 80,147,120-80,147,284 MSH3
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5898787copy number variation1nstd209human GRCh38 chr5: 80,693,345-80,693,470 , GRCh37.p13 chr5: 79,989,164-79,989,289 MSH3
    nsv5896275copy number variation1nstd209human GRCh38 chr5: 80,692,203-80,692,552 , GRCh37.p13 chr5: 79,988,022-79,988,371 MSH3
    nsv5894586copy number variation1nstd209human GRCh38 chr5: 80,743,552-80,743,860 , GRCh37.p13 chr5: 80,039,371-80,039,679 MSH3
    nsv5892213copy number variation1nstd209human GRCh38 chr5: 80,824,340-80,824,414 , GRCh37.p13 chr5: 80,120,159-80,120,233 MSH3
    nsv5888047copy number variation1nstd209human GRCh38 chr5: 80,686,332-80,686,848 , GRCh37.p13 chr5: 79,982,151-79,982,667 MSH3
    nsv5722731mobile element insertion2nstd211human GRCh38 chr5: 80,803,538-80,803,538 , GRCh37.p13 chr5: 80,099,357-80,099,357 MSH3
    nsv5719042mobile element insertion2nstd211human GRCh38 chr5: 80,836,754-80,836,754 , GRCh37.p13 chr5: 80,132,573-80,132,573 MSH3
    nsv5715983mobile element insertion1nstd211human GRCh38 chr5: 80,786,442-80,786,442 , GRCh37.p13 chr5: 80,082,261-80,082,261 MSH3
    nsv5715336mobile element insertion1nstd211human GRCh38 chr5: 80,790,368-80,790,368 , GRCh37.p13 chr5: 80,086,187-80,086,187 MSH3
    nsv5680806mobile element insertion1nstd211human GRCh38 chr5: 80,716,345-80,716,345 , GRCh37.p13 chr5: 80,012,164-80,012,164 MSH3
    nsv5680135mobile element insertion2nstd211human GRCh38 chr5: 80,786,929-80,786,929 , GRCh37.p13 chr5: 80,082,748-80,082,748 MSH3
    nsv5679679mobile element insertion1nstd211human GRCh38 chr5: 80,818,379-80,818,379 , GRCh37.p13 chr5: 80,114,198-80,114,198 MSH3
    nsv5678246mobile element insertion1nstd211human GRCh38 chr5: 80,813,785-80,813,785 , GRCh37.p13 chr5: 80,109,604-80,109,604 MSH3
    nsv5674299delins1nstd102humanPathogenic GRCh37 chr5: 80,021,343-80,021,351 , GRCh38 chr5: 80,725,524-80,725,532 MSH3
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