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Items: 1 to 20 of 214

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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
    nsv7097176copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,441,236-119,252,888 , GRCh38.p12 chr6: 116,120,073-118,931,723 RN7SKP18, COL10A1, 49 more genes
    nsv7051708inversion1nstd229human GRCh38 chr6: 115,507,946-121,145,291 , GRCh37.p13 chr6: 115,829,110-121,466,437 COL10A1, KRT18P22, 67 more genes
    nsv7043912inversion1nstd229human GRCh38 chr6: 113,606,593-119,197,751 , GRCh37.p13 chr6: 113,927,795-119,518,916 TPI1P3, CALHM5, 73 more genes
    nsv6814609copy number variation1nstd229human GRCh38 chr6: 116,568,787-116,583,280 , GRCh37.p13 chr6: 116,889,950-116,904,443 RWDD1
    nsv6810572copy number variation1nstd229human GRCh38 chr6: 116,018,631-116,666,979 , GRCh37.p13 chr6: 116,339,794-116,988,142 FRK, TPI1P3, 18 more genes
    nsv6637080copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,787,149-116,953,270 , GRCh38.p12 chr6: 116,465,986-116,632,107 RSPH4A, CALHM4, 3 more genes
    nsv6614485copy number variation1nstd223human GRCh38 chr6: 116,547,701-116,577,500 , GRCh37.p13 chr6: 116,868,864-116,898,663 CALHM4, RWDD1
    nsv6614318copy number variation1nstd223human GRCh38 chr6: 116,581,801-116,582,500 , GRCh37.p13 chr6: 116,902,964-116,903,663 RWDD1
    nsv6612022copy number variation1nstd223human GRCh38 chr6: 116,586,101-116,587,000 , GRCh37.p13 chr6: 116,907,264-116,908,163 RWDD1
    nsv6606808copy number variation1nstd223human GRCh38 chr6: 111,642,175-118,933,374 , GRCh37.p13 chr6: 111,963,378-119,254,539 COL10A1, LOC105377952, 106 more genes
    nsv6606277copy number variation1nstd223human GRCh38 chr6: 116,586,080-116,597,205 , GRCh37.p13 chr6: 116,907,243-116,918,368 RSPH4A, RWDD1
    nsv6604401copy number variation1nstd223human GRCh38 chr6: 116,580,701-116,582,600 , GRCh37.p13 chr6: 116,901,864-116,903,763 RWDD1
    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
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313666copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,212,698-119,482,708 , GRCh38.p12 chr6: 115,891,534-119,161,543 FAM184A, LOC107986523, 53 more genes
    nsv6257066mobile element insertion1nstd215human GRCh38 chr6: 116,577,523-116,577,523 , GRCh37.p13 chr6: 116,898,686-116,898,686 RWDD1
    nsv6257065mobile element insertion1nstd215human GRCh38 chr6: 116,577,105-116,577,105 , GRCh37.p13 chr6: 116,898,268-116,898,268 RWDD1
    nsv6136164copy number variation1nstd213human GRCh37 chr6: 116,520,000-117,620,001 , GRCh38.p12 chr6: 116,198,837-117,298,838 COL10A1, KPNA5, 26 more genes
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