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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
    nsv7093673copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,564,154-128,786,626 , GRCh38.p12 chr11: 128,694,259-128,916,731 FLI1, KCNJ1, 4 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
    nsv7069138inversion1nstd229human GRCh38 chr11: 128,470,446-128,811,017 , GRCh37.p13 chr11: 128,340,341-128,680,912 SENCR, LOC101929538, 6 more genes
    nsv7063115inversion1nstd229human GRCh38 chr11: 128,798,940-128,798,987 , GRCh37.p13 chr11: 128,668,835-128,668,882 FLI1
    nsv6915247copy number variation1nstd229human GRCh38 chr11: 128,748,401-128,754,100 , GRCh37.p13 chr11: 128,618,296-128,623,995 FLI1
    nsv6913389copy number variation1nstd229human GRCh38 chr11: 128,749,860-128,753,163 , GRCh37.p13 chr11: 128,619,755-128,623,058 FLI1
    nsv6913309copy number variation1nstd229human GRCh38 chr11: 128,790,951-128,793,192 , GRCh37.p13 chr11: 128,660,846-128,663,087 FLI1
    nsv6912557copy number variation1nstd229human GRCh38 chr11: 128,683,527-128,686,820 , GRCh37.p13 chr11: 128,553,422-128,556,715 FLI1, LOC101929538
    nsv6912205copy number variation1nstd229human GRCh38 chr11: 128,538,001-129,014,800 , GRCh37.p13 chr11: 128,407,896-128,884,695 KCNJ1, KCNJ5-AS1, 11 more genes
    nsv6911733copy number variation1nstd229human GRCh38 chr11: 128,740,649-128,970,889 , GRCh37.p13 chr11: 128,610,544-128,840,784 ARHGAP32, LOC107984409, 5 more genes
    nsv6911503copy number variation1nstd229human GRCh38 chr11: 128,782,714-128,788,419 , GRCh37.p13 chr11: 128,652,609-128,658,314 FLI1
    nsv6908501copy number variation1nstd229human GRCh38 chr11: 128,812,462-129,027,216 , GRCh37.p13 chr11: 128,682,357-128,897,111 ARHGAP32, RNU6-876P, 6 more genes
    nsv6904808copy number variation1nstd229human GRCh38 chr11: 128,703,944-128,997,953 , GRCh37.p13 chr11: 128,573,839-128,867,848 KCNJ1, LOC107984409, 6 more genes
    nsv6902860copy number variation1nstd229human GRCh38 chr11: 128,715,133-128,719,202 , GRCh37.p13 chr11: 128,585,028-128,589,097 FLI1
    nsv6899526copy number variation1nstd229human GRCh38 chr11: 128,694,428-128,695,090 , GRCh37.p13 chr11: 128,564,323-128,564,985 FLI1, SENCR
    nsv6899487copy number variation1nstd229human GRCh38 chr11: 128,812,821-128,813,515 , GRCh37.p13 chr11: 128,682,716-128,683,410 FLI1
    nsv6638048copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,682,955-128,897,053 , GRCh38.p12 chr11: 128,813,060-129,027,158 RNU6-876P, ARHGAP32, 6 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
    nsv6637508copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,683,208-128,897,053 , GRCh38.p12 chr11: 128,813,313-129,027,158 KCNJ5, ARHGAP32, 6 more genes
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