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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5913858copy number variation1nstd209human GRCh38 chr12: 12,618,186-12,618,265 , GRCh37.p13 chr12: 12,771,120-12,771,199 CREBL2
    nsv5701119mobile element insertion1nstd211human GRCh38 chr12: 12,625,091-12,625,091 , GRCh37.p13 chr12: 12,778,025-12,778,025 CREBL2
    nsv5695693mobile element insertion1nstd211human GRCh38 chr12: 12,641,277-12,641,277 , GRCh37.p13 chr12: 12,794,211-12,794,211 CREBL2
    nsv5511751copy number variation1nstd206human GRCh38 chr12: 12,618,214-12,618,266 , GRCh37.p13 chr12: 12,771,148-12,771,200 CREBL2
    nsv5505899copy number variation1nstd206human GRCh38 chr12: 12,629,926-12,629,995 , GRCh37.p13 chr12: 12,782,860-12,782,929 CREBL2
    nsv5417382mobile element insertion1nstd206human GRCh38 chr12: 12,625,091-12,625,121 , GRCh37.p13 chr12: 12,778,025-12,778,055 CREBL2
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5137489mobile element insertion1nstd203human GRCh38 chr12: 12,617,643-12,617,681 , GRCh37.p13 chr12: 12,770,577-12,770,615 CREBL2
    nsv5134231mobile element insertion1nstd203human GRCh38 chr12: 12,625,075-12,625,088 , GRCh37.p13 chr12: 12,778,009-12,778,022 CREBL2
    nsv5122929mobile element insertion1nstd203human GRCh38 chr12: 12,617,640-12,617,681 , GRCh37.p13 chr12: 12,770,574-12,770,615 CREBL2
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4972294copy number variation1nstd200human GRCh38 chr12: 12,617,432-12,618,246 , GRCh37.p13 chr12: 12,770,366-12,771,180 CREBL2
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4843482copy number variation1nstd200human GRCh37 chr12: 12,770,366-12,771,180 , GRCh38.p12 chr12: 12,617,432-12,618,246 CREBL2
    nsv4675174copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,737,824-16,780,886 , GRCh38.p12 chr12: 11,584,890-16,627,952 LOC107001063, RN7SKP162, 89 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4528890copy number variation1nstd166human GRCh37.p13 chr12: 12,771,098-12,771,200 , GRCh38.p12 chr12: 12,618,164-12,618,266 CREBL2
    nsv4509137mobile element insertion1nstd166human GRCh37.p13 chr12: 12,778,009-12,778,009 , GRCh38.p12 chr12: 12,625,075-12,625,075 CREBL2
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4436324complex substitution1nstd102humanUncertain significance GRCh38.p12 chr12: 9,922,177-18,648,019 , GRCh37 chr12: 10,074,776-18,800,953 ARHGDIB, ART4, 181 more genes
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