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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    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
    nsv7042981inversion1nstd229human GRCh38 chr6: 122,939,434-128,158,341 , GRCh37.p13 chr6: 123,260,579-128,479,486 CENPW, VIM2P, 56 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
    nsv6808624copy number variation1nstd229human GRCh38 chr6: 127,278,077-127,309,014 , GRCh37.p13 chr6: 127,599,222-127,630,159 ECHDC1, RNF146
    nsv6808592copy number variation1nstd229human GRCh38 chr6: 127,044,701-127,376,848 , GRCh37.p13 chr6: 127,365,846-127,697,993 RPL5P18, RNF146, 5 more genes
    nsv6804845copy number variation1nstd229human GRCh38 chr6: 127,206,727-127,314,334 , GRCh37.p13 chr6: 127,527,872-127,635,479 RNF146, ECHDC1
    nsv6802759copy number variation1nstd229human GRCh38 chr6: 127,239,374-127,580,387 , GRCh37.p13 chr6: 127,560,519-127,901,532 LOC107986642, MTCL3, 10 more genes
    nsv6800537copy number variation1nstd229human GRCh38 chr6: 127,243,009-127,339,277 , GRCh37.p13 chr6: 127,564,154-127,660,422 RNA5SP217, RNF146, 2 more genes
    nsv6636864copy number variation1nstd102humanUncertain significance GRCh37 chr6: 120,059,951-130,033,233 , GRCh38.p12 chr6: 119,738,805-129,712,088 LOC107986640, ECHDC1, 93 more genes
    nsv6618043copy number variation1nstd223human GRCh38 chr6: 127,280,501-127,281,400 , GRCh37.p13 chr6: 127,601,646-127,602,545 RNF146
    nsv6617519copy number variation1nstd223human GRCh38 chr6: 127,287,884-127,288,084 , GRCh37.p13 chr6: 127,609,029-127,609,229 ECHDC1, RNF146
    nsv6612323copy number variation1nstd223human GRCh38 chr6: 127,256,701-127,272,300 , GRCh37.p13 chr6: 127,577,846-127,593,445 RNF146
    nsv6603138copy number variation1nstd223human GRCh38 chr6: 127,287,901-127,289,800 , GRCh37.p13 chr6: 127,609,046-127,610,945 RNF146, ECHDC1
    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
    nsv6313868copy number variation1nstd102humanPathogenic GRCh37 chr6: 122,839,432-128,801,386 , GRCh38.p12 chr6: 122,518,287-128,480,241 TRMT11, HINT3, 61 more genes
    nsv6303367copy number variation1nstd186human GRCh37 chr6: 127,603,360-127,606,719 , GRCh38.p12 chr6: 127,282,215-127,285,574 RNF146
    nsv6290727copy number variation1nstd102humanPathogenic GRCh37 chr6: 125,037,475-129,494,795 , GRCh38.p12 chr6: 124,716,329-129,173,650 LOC100287856, HEY2-AS1, 56 more genes
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