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Items: 1 to 20 of 119

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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
    nsv6816455copy number variation1nstd229human GRCh38 chr6: 122,691,987-122,746,606 , GRCh37.p13 chr6: 123,013,132-123,067,751 PKIB, RN7SL564P
    nsv6808879copy number variation1nstd229human GRCh38 chr6: 122,726,022-122,744,117 , GRCh37.p13 chr6: 123,047,167-123,065,262 PKIB, RN7SL564P
    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
    nsv6616899copy number variation1nstd223human GRCh38 chr6: 122,745,290-122,745,826 , GRCh37.p13 chr6: 123,066,435-123,066,971 RN7SL564P
    nsv6568941inversion1nstd223human GRCh38 chr6: 120,593,241-123,536,832 , GRCh37.p13 chr6: 120,914,387-123,857,977 RNU4-35P, SMPDL3A, 28 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
    nsv6291288copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 117,441,803-123,349,672 , GRCh38.p12 chr6: 117,120,640-123,028,527 FABP7, GJA1, 61 more genes
    nsv6018013copy number variation1nstd212human GRCh38 chr6: 122,656,911-122,760,233 , GRCh37.p13 chr6: 122,978,056-123,081,378 , FABP7, 2 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4768325copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959 GJA1, RNU4-76P, 80 more genes
    nsv4616331copy number variation1nstd183human GRCh37 chr6: 123,027,077-123,066,276 , GRCh38.p12 chr6: 122,705,932-122,745,131 , PKIB, 1 more genes
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