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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5954223insertion1nstd209human GRCh38 chr2: 85,658,040-85,658,040 , GRCh37.p13 chr2: 85,885,163-85,885,163 SFTPB
    nsv5692115mobile element insertion2nstd211human GRCh38 chr2: 85,658,057-85,658,057 , GRCh37.p13 chr2: 85,885,180-85,885,180 SFTPB
    nsv5618590insertion1nstd207human GRCh38 chr2: 85,666,425-85,666,425 , GRCh37.p13 chr2: 85,893,548-85,893,548 SFTPB
    nsv5573119copy number variation1nstd207human GRCh38 chr2: 85,666,223-85,666,492 , GRCh37.p13 chr2: 85,893,346-85,893,615 SFTPB
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5403239mobile element insertion1nstd206human GRCh38 chr2: 85,658,057-85,658,066 , GRCh37.p13 chr2: 85,885,180-85,885,189 SFTPB
    nsv5385143copy number variation1nstd186human GRCh37 chr2: 85,893,350-85,893,529 , GRCh38.p12 chr2: 85,666,227-85,666,406 SFTPB
    nsv5360876translocation1nstd200human GRCh38 chr2: 85,666,456-85,666,456 , GRCh38 chr2: 85,665,855-85,665,855 , GRCh37.p13 chr2: 85,893,579-85,893,579 , GRCh37.p13 chr2: 85,892,978-85,892,978 SFTPB
    nsv5360875translocation1nstd200human GRCh38 chr2: 85,658,278-85,658,278 , GRCh38 chr2: 85,658,339-85,658,339 , GRCh37.p13 chr2: 85,885,401-85,885,401 , GRCh37.p13 chr2: 85,885,462-85,885,462 SFTPB
    nsv5292440copy number variation1nstd204human GRCh38.p13 chr2: 85,666,150-85,666,523 , GRCh37.p13 chr2: 85,893,273-85,893,646 SFTPB
    nsv5077057mobile element insertion1nstd203human GRCh38 chr2: 85,655,313-85,655,341 , GRCh37.p13 chr2: 85,882,436-85,882,464 SFTPB
    nsv5069030mobile element insertion1nstd203human GRCh38 chr2: 85,658,057-85,658,057 , GRCh37.p13 chr2: 85,885,180-85,885,180 SFTPB
    nsv5067709mobile element insertion1nstd203human GRCh38 chr2: 85,658,040-85,658,057 , GRCh37.p13 chr2: 85,885,163-85,885,180 SFTPB
    nsv5063750mobile element insertion1nstd203human GRCh38 chr2: 85,655,341-85,655,348 , GRCh37.p13 chr2: 85,882,464-85,882,471 SFTPB
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5035361inversion1nstd200human GRCh38 chr2: 85,661,762-85,661,926 , GRCh37.p13 chr2: 85,888,885-85,889,049 SFTPB
    nsv4882306inversion1nstd200human GRCh37 chr2: 85,888,885-85,889,049 , GRCh38.p12 chr2: 85,661,762-85,661,926 SFTPB
    nsv4781630copy number variation1nstd200human GRCh37 chr2: 85,893,350-85,893,529 , GRCh38.p12 chr2: 85,666,227-85,666,406 SFTPB
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