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Items: 1 to 20 of 944

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143835insertion1nstd232human GRCh37.p13 chr18: 46,593,777-46,593,777 , GRCh38.p12 chr18: 49,067,407-49,067,407 DYM
    nsv7139751insertion1nstd232human GRCh37.p13 chr18: 46,690,160-46,690,160 , GRCh38.p12 chr18: 49,163,790-49,163,790 DYM
    nsv7095012copy number variation1nstd102humanUncertain significance GRCh37 chr18: 46,450,976-46,690,177 , GRCh38.p12 chr18: 48,924,606-49,163,807 MIR4744, DYM-AS1, 3 more genes
    nsv7076683inversion1nstd229human GRCh38 chr18: 49,079,013-49,079,061 , GRCh37.p13 chr18: 46,605,383-46,605,431 DYM
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7073421inversion1nstd229human GRCh38 chr18: 49,383,488-49,489,016 , GRCh37.p13 chr18: 46,909,858-47,015,386 C18orf32, SNORD58C, 5 more genes
    nsv7070998inversion1nstd229human GRCh38 chr18: 49,429,599-49,429,688 , GRCh37.p13 chr18: 46,955,969-46,956,058 DYM
    nsv7070488inversion1nstd229human GRCh38 chr18: 49,330,144-49,330,163 , GRCh37.p13 chr18: 46,856,514-46,856,533 DYM
    nsv7067659inversion1nstd229human GRCh38 chr18: 49,424,127-49,431,917 , GRCh37.p13 chr18: 46,950,497-46,958,287 DYM
    nsv7064950inversion1nstd229human GRCh38 chr18: 49,426,149-50,066,271 , GRCh37.p13 chr18: 46,952,519-47,592,641 SRP72P1, C18orf32, 19 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7017591copy number variation1nstd229human GRCh38 chr18: 49,394,709-49,398,110 , GRCh37.p13 chr18: 46,921,079-46,924,480 DYM
    nsv7016905copy number variation1nstd229human GRCh38 chr18: 49,323,618-49,331,653 , GRCh37.p13 chr18: 46,849,988-46,858,023 DYM
    nsv7016186copy number variation1nstd229human GRCh38 chr18: 49,132,825-49,143,667 , GRCh37.p13 chr18: 46,659,195-46,670,037 DYM
    nsv7015791copy number variation1nstd229human GRCh38 chr18: 49,264,499-49,273,225 , GRCh37.p13 chr18: 46,790,869-46,799,595 DYM
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7015575copy number variation1nstd229human GRCh38 chr18: 49,186,340-49,190,387 , GRCh37.p13 chr18: 46,712,710-46,716,757 DYM
    nsv7013074copy number variation1nstd229human GRCh38 chr18: 49,187,901-49,191,600 , GRCh37.p13 chr18: 46,714,271-46,717,970 DYM
    nsv7013066copy number variation1nstd229human GRCh38 chr18: 49,154,399-49,156,899 , GRCh37.p13 chr18: 46,680,769-46,683,269 DYM
    nsv7012340copy number variation1nstd229human GRCh38 chr18: 49,307,637-49,309,667 , GRCh37.p13 chr18: 46,834,007-46,836,037 DYM
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