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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139468insertion1nstd232human GRCh37.p13 chr12: 29,496,216-29,496,216 , GRCh38.p12 chr12: 29,343,283-29,343,283 ERGIC2
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv6934849copy number variation1nstd229human GRCh38 chr12: 29,349,687-29,349,808 , GRCh37.p13 chr12: 29,502,620-29,502,741 ERGIC2
    nsv6920964copy number variation1nstd229human GRCh38 chr12: 29,334,740-29,335,119 , GRCh37.p13 chr12: 29,487,673-29,488,052 FAR2, ERGIC2
    nsv6918534copy number variation1nstd229human GRCh38 chr12: 28,759,136-29,359,851 , GRCh37.p13 chr12: 28,912,069-29,512,784 LOC101928735, LOC100506606, 3 more genes
    nsv6637881copy number variation1nstd102humanUncertain significance GRCh37 chr12: 28,911,901-29,518,739 , GRCh38.p12 chr12: 28,758,968-29,365,806 LOC101928735, LOC100506606, 3 more genes
    nsv6621329copy number variation1nstd224human GRCh37 chr12: 29,502,012-29,582,144 , GRCh38.p12 chr12: 29,349,079-29,429,211 OVCH1, ERGIC2, 1 more genes
    nsv6582784inversion1nstd223human GRCh38 chr12: 29,345,899-29,346,063 , GRCh37.p13 chr12: 29,498,832-29,498,996 ERGIC2
    nsv6473644copy number variation1nstd223human GRCh38 chr12: 29,348,201-29,349,800 , GRCh37.p13 chr12: 29,501,134-29,502,733 ERGIC2
    nsv6472599copy number variation1nstd223human GRCh38 chr12: 29,373,244-29,373,946 , GRCh37.p13 chr12: 29,526,177-29,526,879 ERGIC2
    nsv6472070copy number variation1nstd223human GRCh38 chr12: 29,354,301-29,355,700 , GRCh37.p13 chr12: 29,507,234-29,508,633 ERGIC2
    nsv6468336copy number variation1nstd223human GRCh38 chr12: 29,369,401-29,371,000 , GRCh37.p13 chr12: 29,522,334-29,523,933 ERGIC2
    nsv6466644copy number variation1nstd223human GRCh38 chr12: 29,347,484-29,347,936 , GRCh37.p13 chr12: 29,500,417-29,500,869 ERGIC2
    nsv6466035copy number variation1nstd223human GRCh38 chr12: 29,358,114-29,358,666 , GRCh37.p13 chr12: 29,511,047-29,511,599 ERGIC2
    nsv6465383copy number variation1nstd223human GRCh38 chr12: 29,367,201-29,368,300 , GRCh37.p13 chr12: 29,520,134-29,521,233 ERGIC2
    nsv6465047copy number variation1nstd223human GRCh38 chr12: 29,378,501-29,379,600 , GRCh37.p13 chr12: 29,531,434-29,532,533 ERGIC2
    nsv6464018copy number variation1nstd223human GRCh38 chr12: 29,335,881-29,336,543 , GRCh37.p13 chr12: 29,488,814-29,489,476 FAR2, ERGIC2
    nsv6463199copy number variation1nstd223human GRCh38 chr12: 29,348,836-29,349,271 , GRCh37.p13 chr12: 29,501,769-29,502,204 ERGIC2
    nsv6461153copy number variation1nstd223human GRCh38 chr12: 29,348,001-29,350,300 , GRCh37.p13 chr12: 29,500,934-29,503,233 ERGIC2
    nsv6460960copy number variation1nstd223human GRCh38 chr12: 29,348,070-29,348,557 , GRCh37.p13 chr12: 29,501,003-29,501,490 ERGIC2
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