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Items: 1 to 20 of 120

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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
    nsv6636667copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,522,860-134,541,311 , GRCh38.p12 chr6: 133,201,721-134,220,173 LINC01312, SGK1, 11 more genes
    nsv6606035copy number variation1nstd223human GRCh38 chr6: 133,885,401-133,893,000 , GRCh37.p13 chr6: 134,206,539-134,214,138 TCF21, TARID
    nsv6603505copy number variation1nstd223human GRCh38 chr6: 133,810,537-133,949,378 , GRCh37.p13 chr6: 134,131,675-134,270,516 LINC01312, TCF21, 1 more genes
    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
    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
    nsv6136169copy number variation1nstd213human GRCh37 chr6: 133,310,000-134,340,001 , GRCh38.p12 chr6: 132,988,861-134,018,863 EYA4, TCF21, 10 more genes
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5576383copy number variation1nstd207human GRCh38 chr6: 133,894,736-133,896,214 , GRCh37.p13 chr6: 134,215,874-134,217,352 TCF21
    nsv5470770copy number variation1nstd206human GRCh38 chr6: 133,894,739-133,896,215 , GRCh37.p13 chr6: 134,215,877-134,217,353 TCF21
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945696copy number variation1nstd200human GRCh38 chr6: 133,810,537-133,949,382 , GRCh37.p13 chr6: 134,131,675-134,270,520 TCF21, LINC01312, 1 more genes
    nsv4675250copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264 ALDH8A1, IL22RA2, 99 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
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