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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077992inversion1nstd229human GRCh38 chr11: 133,670,317-134,396,679 , GRCh37.p13 chr11: 133,540,212-134,266,573 THYN1, LINC02731, 17 more genes
    nsv7077828inversion1nstd229human GRCh38 chr11: 133,469,560-134,299,113 , GRCh37.p13 chr11: 133,339,455-134,169,007 SPATA19, LINC02731, 15 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7074032inversion1nstd229human GRCh38 chr11: 133,755,029-134,396,594 , GRCh37.p13 chr11: 133,624,924-134,266,488 SPATA19, LINC02731, 17 more genes
    nsv7072222inversion1nstd229human GRCh38 chr11: 133,293,068-134,631,853 , GRCh37.p13 chr11: 133,162,963-134,501,747 LOC100533644, IGSF9B, 19 more genes
    nsv7068145inversion1nstd229human GRCh38 chr11: 133,349,545-133,930,001 , GRCh37.p13 chr11: 133,219,440-133,799,896 LINC02743, MIR4697, 4 more genes
    nsv7064304inversion1nstd229human GRCh38 chr11: 133,652,192-134,531,094 , GRCh37.p13 chr11: 133,522,087-134,400,988 LOC100533644, VPS26B, 18 more genes
    nsv7061753inversion1nstd229human GRCh38 chr11: 133,844,566-134,176,017 , GRCh37.p13 chr11: 133,714,461-134,045,912 LINC02731, JAM3, 9 more genes
    nsv7058477inversion1nstd229human GRCh38 chr11: 133,842,619-133,894,408 , GRCh37.p13 chr11: 133,712,514-133,764,303 SPATA19, LOC283172
    nsv7058146inversion1nstd229human GRCh38 chr11: 133,828,335-134,640,806 , GRCh37.p13 chr11: 133,698,230-134,510,700 PTP4A2P2, LOC105369583, 18 more genes
    nsv6917046copy number variation1nstd229human GRCh38 chr11: 133,780,158-134,289,607 , GRCh37.p13 chr11: 133,650,053-134,159,501 JAM3, LINC02731, 14 more genes
    nsv6913084copy number variation1nstd229human GRCh38 chr11: 133,402,796-134,336,711 , GRCh37.p13 chr11: 133,272,691-134,206,605 MIR4697, LINC02743, 17 more genes
    nsv6908156copy number variation1nstd229human GRCh38 chr11: 133,620,071-134,431,008 , GRCh37.p13 chr11: 133,489,966-134,300,902 LOC100533644, IGSF9B, 17 more genes
    nsv6906818copy number variation1nstd229human GRCh38 chr11: 133,456,115-134,317,984 , GRCh37.p13 chr11: 133,326,010-134,187,878 JAM3, LINC02731, 16 more genes
    nsv6905822copy number variation1nstd229human GRCh38 chr11: 133,469,601-134,042,900 , GRCh37.p13 chr11: 133,339,496-133,912,795 IGSF9B, OPCML, 6 more genes
    nsv6901855copy number variation1nstd229human GRCh38 chr11: 133,843,808-133,847,592 , GRCh37.p13 chr11: 133,713,703-133,717,487 SPATA19
    nsv6637976copy number variation1nstd102humanUncertain significance GRCh37 chr11: 133,238,757-134,330,730 , GRCh38.p12 chr11: 133,368,862-134,460,836 IGSF9B, GLB1L2, 19 more genes
    nsv6637910copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 130,935,635-134,938,470 , GRCh38.p12 chr11: 131,065,740-135,068,576 OPCML, PTP4A2P2, 38 more genes
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
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