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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054647inversion1nstd229human GRCh38 chr6: 125,609,155-134,343,808 , GRCh37.p13 chr6: 125,930,301-134,664,946 RPS12, TMEM244, 130 more genes
    nsv7053719inversion1nstd229human GRCh38 chr6: 125,606,974-134,343,957 , GRCh37.p13 chr6: 125,928,120-134,665,095 SNORD100, SLC18B1, 130 more genes
    nsv7040961inversion1nstd229human GRCh38 chr6: 131,090,546-134,695,837 , GRCh37.p13 chr6: 131,411,686-135,016,975 ENPP3, MOXD1, 70 more genes
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6815001copy number variation1nstd229human GRCh38 chr6: 131,950,167-131,950,291 , GRCh37.p13 chr6: 132,271,307-132,271,431 CCN2
    nsv6811533copy number variation1nstd229human GRCh38 chr6: 131,891,712-132,414,416 , GRCh37.p13 chr6: 132,212,852-132,735,555 MOXD1, LINC01013, 4 more genes
    nsv6808954copy number variation1nstd229human GRCh38 chr6: 131,464,715-132,189,626 , GRCh37.p13 chr6: 131,785,855-132,510,766 LOC100421775, MIR548H5, 14 more genes
    nsv6618587copy number variation1nstd223human GRCh38 chr6: 131,949,301-131,951,600 , GRCh37.p13 chr6: 132,270,441-132,272,740 CCN2
    nsv6563707inversion1nstd223human GRCh38 chr6: 125,606,968-134,343,906 , GRCh37.p13 chr6: 125,928,114-134,665,044 TAAR2, LOC105377996, 130 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6315104copy number variation1nstd102humanPathogenic GRCh38 chr6: 131,688,637-132,215,008 , GRCh37.p13 chr6: 132,009,777-132,536,148 ENPP3, LINC01013, 10 more genes
    nsv6290946copy number variation1nstd102humanPathogenic GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079 LOC105378004, LINC01010, 89 more genes
    nsv6290914copy number variation1nstd102humanUncertain significance GRCh37 chr6: 131,958,038-132,444,269 , GRCh38.p12 chr6: 131,636,898-132,123,129 MIR548AJ1, ENPP1, 10 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4608753copy number variation1nstd183human GRCh37 chr6: 132,271,812-132,272,413 , GRCh38.p12 chr6: 131,950,672-131,951,273 CCN2
    nsv4456062copy number variation1nstd102humanUncertain significance GRCh37 chr6: 131,958,069-132,444,234 , GRCh38.p12 chr6: 131,636,929-132,123,094 ENPP3, RNU4-18P, 10 more genes
    nsv4455443copy number variation1nstd102humanUncertain significance GRCh37 chr6: 131,673,206-132,706,248 , GRCh38.p12 chr6: 131,352,066-132,385,109 CTAGE9, SELENOKP2, 17 more genes
    nsv4349636copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 129,513,837-132,618,991 , GRCh38.p12 chr6: 129,192,692-132,297,852 ARG1, CCN2, 37 more genes
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