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Items: 1 to 20 of 176

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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
    nsv7142231insertion1nstd232human GRCh37.p13 chr6: 125,598,384-125,598,384 , GRCh38.p12 chr6: 125,277,238-125,277,238 HDDC2
    nsv7093381copy number variation1nstd102humannot provided GRCh37 chr6: 119,243,634-126,078,530 , GRCh38.p12 chr6: 118,922,469-125,757,384 HEY2-AS1, SERINC1, 52 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
    nsv6812259copy number variation1nstd229human GRCh38 chr6: 125,301,801-125,316,300 , GRCh37.p13 chr6: 125,622,947-125,637,446 HDDC2
    nsv6811940copy number variation1nstd229human GRCh38 chr6: 125,280,495-125,286,450 , GRCh37.p13 chr6: 125,601,641-125,607,596 HDDC2
    nsv6806585copy number variation1nstd229human GRCh38 chr6: 125,206,057-125,293,257 , GRCh37.p13 chr6: 125,527,203-125,614,403 HDDC2, TPD52L1
    nsv6805632copy number variation1nstd229human GRCh38 chr6: 125,216,194-125,444,830 , GRCh37.p13 chr6: 125,537,340-125,765,976 LOC107986640, TPD52L1, 2 more genes
    nsv6799252copy number variation1nstd229human GRCh38 chr6: 125,057,864-125,367,194 , GRCh37.p13 chr6: 125,379,010-125,688,340 TPD52L1, HDDC2, 4 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
    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
    nsv6135232copy number variation1nstd213human GRCh37 chr6: 125,470,000-125,650,001 , GRCh38.p12 chr6: 125,148,854-125,328,855 TPD52L1, HDDC2, 1 more genes
    nsv5966419insertion1nstd209human GRCh38 chr6: 125,301,481-125,301,481 , GRCh37.p13 chr6: 125,622,627-125,622,627 HDDC2
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5728842mobile element insertion1nstd211human GRCh38 chr6: 125,289,494-125,289,494 , GRCh37.p13 chr6: 125,610,640-125,610,640 HDDC2
    nsv5687050mobile element insertion1nstd211human GRCh38 chr6: 125,274,958-125,274,958 , GRCh37.p13 chr6: 125,596,104-125,596,104 HDDC2
    nsv5643708insertion1nstd207human GRCh38 chr6: 125,301,481-125,301,481 , GRCh37.p13 chr6: 125,622,627-125,622,627 HDDC2
    nsv5551665insertion1nstd206human GRCh38 chr6: 125,301,503-125,301,532 , GRCh37.p13 chr6: 125,622,649-125,622,678 HDDC2
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