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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137662copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 112,103,088-112,128,142 , GRCh38.p12 chr5: 112,767,391-112,792,445 APC, CBX3P3, 1 more genes
    nsv6112677copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 112,175,770-112,176,559 , GRCh38 chr5: 112,840,073-112,840,862 APC
    nsv5980433copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,090,568-112,179,843 , GRCh38.p12 chr5: 112,754,871-112,844,146 CBX3P3, RNU6-482P, 1 more genes
    nsv5951727insertion1nstd209human GRCh38 chr5: 112,717,908-112,717,908 , GRCh37.p13 chr5: 112,053,605-112,053,605 APC
    nsv5901898copy number variation1nstd209human GRCh38 chr5: 112,726,098-112,726,213 , GRCh37.p13 chr5: 112,061,795-112,061,910 APC
    nsv5888049copy number variation1nstd209human GRCh38 chr5: 112,797,371-112,800,791 , GRCh37.p13 chr5: 112,133,068-112,136,488 APC
    nsv5840362copy number variation1nstd209human GRCh38 chr5: 112,797,312-112,800,311 , GRCh37.p13 chr5: 112,133,009-112,136,008 APC
    nsv5840361copy number variation1nstd209human GRCh38 chr5: 112,751,523-112,753,572 , GRCh37.p13 chr5: 112,087,220-112,089,269 APC
    nsv5840360copy number variation1nstd209human GRCh38 chr5: 112,710,263-112,711,362 , GRCh37.p13 chr5: 112,045,960-112,047,059 APC
    nsv5723998mobile element insertion2nstd211human GRCh38 chr5: 112,845,601-112,845,601 , GRCh37.p13 chr5: 112,181,298-112,181,298 APC
    nsv5674314insertion1nstd102humanPathogenic GRCh37 chr5: 112,175,856-112,175,856 , GRCh38 chr5: 112,840,159-112,840,159 APC
    nsv5674273insertion1nstd102humanPathogenic GRCh37 chr5: 112,175,358-112,175,358 , GRCh38 chr5: 112,839,661-112,839,661 APC
    nsv5674252delins1nstd102humanPathogenic GRCh37 chr5: 112,174,379-112,174,383 , GRCh38 chr5: 112,838,682-112,838,686 APC
    nsv5673750copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,043,009-112,151,296 , GRCh38.p12 chr5: 112,707,312-112,815,599 APC, RNU6-482P, 1 more genes
    nsv5673656copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 112,090,582-112,137,086 , GRCh38.p12 chr5: 112,754,885-112,801,389 APC, CBX3P3, 1 more genes
    nsv5673503copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,154,657-112,179,828 , GRCh38.p12 chr5: 112,818,960-112,844,131 APC
    nsv5673502copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,154,657-112,157,694 , GRCh38.p12 chr5: 112,818,960-112,821,997 APC
    nsv5673501copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,151,175-112,155,051 , GRCh38.p12 chr5: 112,815,478-112,819,354 APC
    nsv5673500copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,111,314-112,111,444 , GRCh38.p12 chr5: 112,775,617-112,775,747 CBX3P3, APC
    nsv5673499copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 112,090,582-112,157,694 , GRCh38.p12 chr5: 112,754,885-112,821,997 APC, CBX3P3, 1 more genes
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