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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6694281copy number variation1nstd229human GRCh38 chr2: 134,910,646-134,975,494 , GRCh37.p13 chr2: 135,668,216-135,733,064 CCNT2, MAP3K19, 1 more genes
    nsv6689998copy number variation1nstd229human GRCh38 chr2: 134,880,102-134,889,099 , GRCh37.p13 chr2: 135,637,672-135,646,669 CCNT2-AS1, ACMSD
    nsv6685941copy number variation1nstd229human GRCh38 chr2: 134,868,183-134,876,491 , GRCh37.p13 chr2: 135,625,753-135,634,061 ACMSD, CCNT2-AS1
    nsv6682162copy number variation1nstd229human GRCh38 chr2: 134,860,001-134,895,900 , GRCh37.p13 chr2: 135,617,571-135,653,470 CCNT2-AS1, ACMSD
    nsv6682102copy number variation1nstd229human GRCh38 chr2: 134,880,553-134,884,830 , GRCh37.p13 chr2: 135,638,123-135,642,400 ACMSD, CCNT2-AS1
    nsv6681094copy number variation1nstd229human GRCh38 chr2: 134,890,247-134,895,133 , GRCh37.p13 chr2: 135,647,817-135,652,703 ACMSD, CCNT2-AS1
    nsv6679692copy number variation1nstd229human GRCh38 chr2: 128,625,642-138,426,614 , GRCh37.p13 chr2: 129,383,216-139,184,184 MTND4P27, LOC646674, 194 more genes
    nsv6348614copy number variation1nstd223human GRCh38 chr2: 134,889,801-134,892,000 , GRCh37.p13 chr2: 135,647,371-135,649,570 ACMSD, CCNT2-AS1
    nsv6343109copy number variation1nstd223human GRCh38 chr2: 128,625,639-138,426,614 , GRCh37.p13 chr2: 129,383,213-139,184,184 CYP4F30P, CCDC74B, 194 more genes
    nsv6342997copy number variation1nstd223human GRCh38 chr2: 134,914,967-134,916,145 , GRCh37.p13 chr2: 135,672,537-135,673,715 CCNT2-AS1
    nsv6339824copy number variation1nstd223human GRCh38 chr2: 134,899,201-134,900,100 , GRCh37.p13 chr2: 135,656,771-135,657,670 CCNT2-AS1, ACMSD
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6298574copy number variation1nstd186human GRCh37 chr2: 135,652,885-135,652,940 , GRCh38.p12 chr2: 134,895,315-134,895,370 CCNT2-AS1, ACMSD
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6290867copy number variation1nstd102humanPathogenic GRCh37 chr2: 122,699,106-143,799,629 , GRCh38.p12 chr2: 121,941,530-143,042,060 RNU6-675P, RNU6-1049P, 300 more genes
    nsv6275917insertion1nstd214human GRCh38 chr2: 134,918,497-134,918,497 , GRCh37.p13 chr2: 135,676,067-135,676,067 CCNT2, CCNT2-AS1
    nsv6154996copy number variation1nstd214human GRCh38 chr2: 134,903,816-134,903,974 , GRCh37.p13 chr2: 135,661,386-135,661,544 CCNT2-AS1
    nsv6149287copy number variation1nstd214human GRCh38 chr2: 134,903,840-134,903,998 , GRCh37.p13 chr2: 135,661,410-135,661,568 CCNT2-AS1
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