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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117686mobile element insertion1nstd186human GRCh37 chr7: 105,635,799-105,635,804 , GRCh38.p12 chr7: 105,995,353-105,995,358 CDHR3
    nsv6116929mobile element insertion1nstd186human GRCh37 chr7: 105,564,465-105,564,516 , GRCh38.p12 chr7: 105,924,019-105,924,070 CDHR3
    nsv5951244insertion1nstd209human GRCh38 chr7: 105,924,009-105,924,009 , GRCh37.p13 chr7: 105,564,455-105,564,455 CDHR3
    nsv5923169copy number variation1nstd209human GRCh38 chr7: 105,893,609-105,894,082 , GRCh37.p13 chr7: 105,534,055-105,534,528 CDHR3
    nsv5919624copy number variation1nstd209human GRCh38 chr7: 105,994,221-105,994,291 , GRCh37.p13 chr7: 105,634,667-105,634,737 CDHR3
    nsv5727843mobile element insertion1nstd211human GRCh38 chr7: 106,017,148-106,017,148 , GRCh37.p13 chr7: 105,657,594-105,657,594 CDHR3
    nsv5727620mobile element insertion1nstd211human GRCh38 chr7: 105,875,637-105,875,637 , GRCh37.p13 chr7: 105,516,083-105,516,083 CDHR3, ATXN7L1
    nsv5691533mobile element insertion2nstd211human GRCh38 chr7: 105,995,353-105,995,353 , GRCh37.p13 chr7: 105,635,799-105,635,799 CDHR3
    nsv5679219mobile element insertion2nstd211human GRCh38 chr7: 105,924,019-105,924,019 , GRCh37.p13 chr7: 105,564,465-105,564,465 CDHR3
    nsv5643314insertion1nstd207human GRCh38 chr7: 105,995,348-105,995,348 , GRCh37.p13 chr7: 105,635,794-105,635,794 CDHR3
    nsv5635078insertion2nstd207human GRCh38 chr7: 105,908,615-105,908,615 , GRCh37.p13 chr7: 105,549,061-105,549,061 CDHR3
    nsv5627588insertion1nstd207human GRCh38 chr7: 105,924,009-105,924,009 , GRCh37.p13 chr7: 105,564,455-105,564,455 CDHR3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5490701copy number variation1nstd206human GRCh38 chr7: 105,961,205-105,961,305 , GRCh37.p13 chr7: 105,601,651-105,601,751 CDHR3
    nsv5488742copy number variation1nstd206human GRCh38 chr7: 105,896,052-105,896,103 , GRCh37.p13 chr7: 105,536,498-105,536,549 CDHR3
    nsv5483998copy number variation1nstd206human GRCh38 chr7: 105,982,101-105,982,167 , GRCh37.p13 chr7: 105,622,547-105,622,613 CDHR3
    nsv5478356copy number variation1nstd206human GRCh38 chr7: 105,908,514-105,908,589 , GRCh37.p13 chr7: 105,548,960-105,549,035 CDHR3
    nsv5403245mobile element insertion1nstd206human GRCh38 chr7: 105,995,353-105,995,358 , GRCh37.p13 chr7: 105,635,799-105,635,804 CDHR3
    nsv5400963mobile element insertion1nstd206human GRCh38 chr7: 105,924,019-105,924,070 , GRCh37.p13 chr7: 105,564,465-105,564,516 CDHR3
    nsv5370933translocation1nstd200human GRCh38 chr7: 105,973,098-105,973,098 , GRCh38 chr7: 105,974,257-105,974,257 , GRCh37.p13 chr7: 105,613,544-105,613,544 , GRCh37.p13 chr7: 105,614,703-105,614,703 CDHR3
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