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Items: 1 to 20 of 112

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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
    nsv7050313inversion1nstd229human GRCh38 chr6: 126,416,318-126,695,388 , GRCh37.p13 chr6: 126,737,464-127,016,533 MIR588, PRELID1P1, 7 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
    nsv7042628inversion1nstd229human GRCh38 chr6: 126,416,319-126,513,393 , GRCh37.p13 chr6: 126,737,465-126,834,539 CENPW, MIR588
    nsv7038109inversion1nstd229human GRCh38 chr6: 125,606,921-134,343,957 , GRCh37.p13 chr6: 125,928,067-134,665,095 PTPRK-AS1, MED23, 130 more genes
    nsv6814381copy number variation1nstd229human GRCh38 chr6: 126,445,028-126,588,082 , GRCh37.p13 chr6: 126,766,174-126,909,228 MIR588, CENPW
    nsv6801306copy number variation1nstd229human GRCh38 chr6: 126,483,330-126,502,231 , GRCh37.p13 chr6: 126,804,476-126,823,377 MIR588, CENPW
    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
    nsv6603706copy number variation1nstd223human GRCh38 chr6: 126,482,401-126,483,400 , GRCh37.p13 chr6: 126,803,547-126,804,546 MIR588, CENPW
    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
    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
    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
    nsv5458832copy number variation1nstd206human GRCh38 chr6: 126,370,926-127,424,730 , GRCh37.p13 chr6: 126,692,072-127,745,875 , YWHAZP4, 19 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4933971copy number variation1nstd200human GRCh38 chr6: 126,448,145-126,553,059 , GRCh37.p13 chr6: 126,769,291-126,874,205 CENPW, MIR588
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