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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv1744767copy number variation1estd22human NCBI36 chr3: 42,949,505-42,949,506 , GRCh37.p13 chr3: 42,974,501-42,974,502 , GRCh38.p12 chr3: 42,933,009-42,933,010 KRBOX1-AS1
    nsv2163330short tandem repeat5nstd128human GRCh37 chr3: 42,974,485-42,974,502 , GRCh38.p12 chr3: 42,932,993-42,933,010 KRBOX1-AS1
    nsv2167117short tandem repeat1nstd128human GRCh37 chr3: 42,975,625-42,975,640 , GRCh38.p12 chr3: 42,934,133-42,934,148 KRBOX1-AS1
    nsv2167116short tandem repeat1nstd128human GRCh37 chr3: 42,974,905-42,974,917 , GRCh38.p12 chr3: 42,933,413-42,933,425 KRBOX1-AS1
    nsv6714086copy number variation1nstd229human GRCh38 chr3: 42,930,872-42,936,905 , GRCh37.p13 chr3: 42,972,364-42,978,397 KRBOX1, KRBOX1-AS1
    nsv5061299mobile element insertion1nstd203human GRCh38 chr3: 42,937,017-42,937,032 , GRCh37.p13 chr3: 42,978,509-42,978,524 KRBOX1, KRBOX1-AS1
    nsv6067782insertion1nstd212human GRCh38 chr3: 42,937,015-42,937,015 , GRCh37.p13 chr3: 42,978,507-42,978,507 KRBOX1, KRBOX1-AS1
    nsv4470945mobile element insertion1nstd166human GRCh37.p13 chr3: 42,978,507-42,978,507 , GRCh38.p12 chr3: 42,937,015-42,937,015 KRBOX1, KRBOX1-AS1
    nsv3186808complex substitution1nstd152human GRCh38 chr3: 42,936,606-42,936,665 , GRCh37.p13 chr3: 42,978,098-42,978,157 KRBOX1, KRBOX1-AS1
    nsv2167118short tandem repeat1nstd128human GRCh37 chr3: 42,976,410-42,976,427 , GRCh38.p12 chr3: 42,934,918-42,934,935 KRBOX1, KRBOX1-AS1
    nsv590149copy number variation1nstd54human NCBI36 chr3: 42,942,601-43,150,211 , GRCh37.p13 chr3: 42,967,597-43,175,207 , GRCh38.p12 chr3: 42,926,105-43,133,715 KRBOX1, KRBOX1-AS1, 3 more genes
    nsv460522copy number variation1nstd27human NCBI35 chr3: 42,942,601-43,150,211 , GRCh37.p13 chr3: 42,967,597-43,175,207 , GRCh38.p12 chr3: 42,926,105-43,133,715 KRBOX1, LOC107986079, 3 more genes
    nsv3881275copy number variation1nstd102humanPathogenic GRCh37 chr3: 41,104,508-44,636,698 , GRCh38.p12 chr3: 41,063,017-44,595,206 KRBOX1, LOC107986077, 69 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 KRBOX1, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 KRBOX1, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 KRBOX1, RPL23AP49, 2875 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 KRBOX1, RNU6-243P, 382 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 KRBOX1, ACAA1, 344 more genes
    nsv429644copy number variation1nstd11human GRCh37.p13 chr3: 35,009,045-84,383,151 , GRCh38.p12 chr3: 34,967,553-84,334,000 , NCBI36 chr3: 34,984,049-84,465,841 KRBOX1, ACAA1, 823 more genes
    nsv6311795copy number variation1nstd102humanUncertain significance GRCh37 chr3: 40,924,962-43,760,024 , GRCh38.p12 chr3: 40,883,471-43,718,532 KRBOX1, VIPR1, 52 more genes
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