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Items: 1 to 20 of 133

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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
    nsv7050464inversion1nstd229human GRCh38 chr6: 127,449,003-127,449,064 , GRCh37.p13 chr6: 127,770,148-127,770,209 MTCL3, KIAA0408
    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
    nsv6813400copy number variation1nstd229human GRCh38 chr6: 127,338,601-127,445,800 , GRCh37.p13 chr6: 127,659,746-127,766,945 RPL5P18, LOC100287856, 6 more genes
    nsv6806814copy number variation1nstd229human GRCh38 chr6: 127,342,001-127,441,200 , GRCh37.p13 chr6: 127,663,146-127,762,345 RPL5P18, MTCL3, 6 more genes
    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
    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
    nsv6614716copy number variation1nstd223human GRCh38 chr6: 127,454,564-127,454,997 , GRCh37.p13 chr6: 127,775,709-127,776,142 KIAA0408, MTCL3
    nsv6612968copy number variation1nstd223human GRCh38 chr6: 127,450,682-127,451,247 , GRCh37.p13 chr6: 127,771,827-127,772,392 KIAA0408, MTCL3
    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
    nsv5974647inversion1nstd209human GRCh38 chr6: 127,434,769-127,509,002 , GRCh37.p13 chr6: 127,755,914-127,830,147 KIAA0408, MTCL3, 2 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
    nsv5894472copy number variation1nstd209human GRCh38 chr6: 127,447,593-127,447,645 , GRCh37.p13 chr6: 127,768,738-127,768,790 KIAA0408, MTCL3
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