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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980418copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,639,700-47,643,434 , GRCh38.p12 chr2: 47,412,561-47,416,295 MSH2
    nsv5980416copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,635,695-47,639,552 , GRCh38.p12 chr2: 47,408,556-47,412,413 MSH2
    nsv5980394copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,635,695-47,690,169 , GRCh38.p12 chr2: 47,408,556-47,463,030 MSH2
    nsv5961824insertion1nstd209human GRCh38 chr2: 47,582,849-47,582,849 , GRCh37.p13 chr2: 47,809,988-47,809,988 MSH2
    nsv5961005insertion1nstd209human GRCh38 chr2: 47,449,026-47,449,026 , GRCh37.p13 chr2: 47,676,165-47,676,165 MSH2
    nsv5952256insertion1nstd209human GRCh38 chr2: 47,502,621-47,502,621 , GRCh37.p13 chr2: 47,729,760-47,729,760 MSH2
    nsv5887298copy number variation1nstd209human GRCh38 chr2: 47,531,237-47,534,126 , GRCh37.p13 chr2: 47,758,376-47,761,265 MSH2, KCNK12
    nsv5877881copy number variation1nstd209human GRCh38 chr2: 47,415,160-47,415,226 , GRCh37.p13 chr2: 47,642,299-47,642,365 MSH2
    nsv5874139copy number variation1nstd209human GRCh38 chr2: 47,420,712-47,424,587 , GRCh37.p13 chr2: 47,647,851-47,651,726 MSH2
    nsv5873335copy number variation1nstd209human GRCh38 chr2: 47,426,917-47,426,995 , GRCh37.p13 chr2: 47,654,056-47,654,134 MSH2
    nsv5872058copy number variation1nstd209human GRCh38 chr2: 47,447,734-47,447,833 , GRCh37.p13 chr2: 47,674,873-47,674,972 MSH2
    nsv5833366copy number variation1nstd209human GRCh38 chr2: 47,479,016-47,480,553 , GRCh37.p13 chr2: 47,706,155-47,707,692 MSH2
    nsv5833272copy number variation1nstd209human GRCh38 chr2: 47,531,223-47,534,022 , GRCh37.p13 chr2: 47,758,362-47,761,161 KCNK12, MSH2
    nsv5833271copy number variation1nstd209human GRCh38 chr2: 47,420,424-47,428,040 , GRCh37.p13 chr2: 47,647,563-47,655,179 MSH2
    nsv5728669mobile element insertion2nstd211human GRCh38 chr2: 47,582,865-47,582,865 , GRCh37.p13 chr2: 47,810,004-47,810,004 MSH2
    nsv5674278insertion1nstd102humanPathogenic GRCh37 chr2: 47,702,376-47,702,376 , GRCh38 chr2: 47,475,237-47,475,237 MSH2
    nsv5673710copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr2: 47,690,160-47,693,957 , GRCh38.p12 chr2: 47,463,021-47,466,818 MSH2
    nsv5673709copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,656,871-47,710,120 , GRCh38.p12 chr2: 47,429,732-47,482,981 MSH2
    nsv5673708copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr2: 47,656,871-47,698,211 , GRCh38.p12 chr2: 47,429,732-47,471,072 MSH2
    nsv5673707copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,637,223-47,672,806 , GRCh38.p12 chr2: 47,410,084-47,445,667 MSH2
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