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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
    nsv7137202copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,713,854-124,105,184 , GRCh38.p12 chr6: 112,392,652-123,784,039 COL10A1, FABP7, 129 more genes
    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
    nsv7052079inversion1nstd229human GRCh38 chr6: 119,644,000-123,115,000 , GRCh37.p13 chr6: 119,965,161-123,436,145 RNA5SP215, RNU4-35P, 28 more genes
    nsv7051442inversion1nstd229human GRCh38 chr6: 120,525,437-125,245,762 , GRCh37.p13 chr6: 120,846,583-125,566,908 RNF217-AS1, HSF2, 35 more genes
    nsv7048680inversion1nstd229human GRCh38 chr6: 120,128,256-123,693,128 , GRCh37.p13 chr6: 120,449,402-124,014,273 TRDN-AS1, TBC1D32, 30 more genes
    nsv6817028copy number variation1nstd229human GRCh38 chr6: 118,002,640-125,132,407 , GRCh37.p13 chr6: 118,323,803-125,453,553 GJA1, COX6A1P3, 56 more genes
    nsv6811486copy number variation1nstd229human GRCh38 chr6: 122,403,908-122,408,497 , GRCh37.p13 chr6: 122,725,053-122,729,642 HSF2
    nsv6636964copy number variation1nstd102humanUncertain significance GRCh37 chr6: 121,646,369-124,675,332 , GRCh38.p12 chr6: 121,325,223-124,354,186 HMGN2P29, ATP5MGP2, 27 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
    nsv6617739copy number variation1nstd223human GRCh38 chr6: 122,411,418-122,412,094 , GRCh37.p13 chr6: 122,732,563-122,733,239 HSF2
    nsv6613908copy number variation1nstd223human GRCh38 chr6: 122,426,246-122,426,911 , GRCh37.p13 chr6: 122,747,391-122,748,056 HSF2
    nsv6613410copy number variation1nstd223human GRCh38 chr6: 122,427,155-122,427,505 , GRCh37.p13 chr6: 122,748,300-122,748,650 HSF2
    nsv6613405copy number variation1nstd223human GRCh38 chr6: 122,424,936-122,425,518 , GRCh37.p13 chr6: 122,746,081-122,746,663 HSF2
    nsv6612886copy number variation1nstd223human GRCh38 chr6: 122,423,901-122,424,900 , GRCh37.p13 chr6: 122,745,046-122,746,045 HSF2
    nsv6609128copy number variation1nstd223human GRCh38 chr6: 122,413,859-122,415,118 , GRCh37.p13 chr6: 122,735,004-122,736,263 HSF2
    nsv6608518copy number variation1nstd223human GRCh38 chr6: 122,427,701-122,429,500 , GRCh37.p13 chr6: 122,748,846-122,750,645 HSF2
    nsv6568941inversion1nstd223human GRCh38 chr6: 120,593,241-123,536,832 , GRCh37.p13 chr6: 120,914,387-123,857,977 RNU4-35P, SMPDL3A, 28 more genes
    nsv6557595inversion1nstd223human GRCh38 chr6: 122,402,564-122,403,590 , GRCh37.p13 chr6: 122,723,709-122,724,735 HSF2
    nsv6555950inversion1nstd223human GRCh38 chr6: 122,414,826-122,415,733 , GRCh37.p13 chr6: 122,735,971-122,736,878 HSF2
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