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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053970inversion1nstd229human GRCh38 chr6: 112,084,907-112,090,579 , GRCh37.p13 chr6|NW_003871062.1: 82,429-88,101 , GRCh37.p13 chr6: 112,406,110-112,411,782 TUBE1, FAM229B
    nsv7040236inversion1nstd229human GRCh38 chr6: 111,756,087-112,191,364 , GRCh37.p13 chr6: 112,077,290-112,323,681 TUBE1, FYN, 7 more genes
    nsv6815317copy number variation1nstd229human GRCh38 chr6: 110,458,576-114,390,336 , GRCh37.p13 chr6: 110,779,779-114,711,500 LOC105377956, LOC102724646, 79 more genes
    nsv6809374copy number variation1nstd229human GRCh38 chr6: 112,046,493-112,158,352 , GRCh37.p13 chr6: 112,367,696-112,479,554 , GRCh37.p13 chr6|NW_003871062.1: 44,015-155,873 CCN6, FAM229B, 3 more genes
    nsv6808751copy number variation1nstd229human GRCh38 chr6: 111,950,266-112,105,602 , GRCh37.p13 chr6|NW_003871062.1: 1-103,124 , GRCh37.p13 chr6: 112,323,682-112,426,805 FAM229B, TUBE1, 2 more genes
    nsv6805072copy number variation1nstd229human GRCh38 chr6: 112,099,707-112,103,043 , GRCh37.p13 chr6|NW_003871062.1: 97,229-100,565 , GRCh37.p13 chr6: 112,420,910-112,424,246 FAM229B
    nsv6803599copy number variation1nstd229human GRCh38 chr6: 112,087,253-112,213,404 , GRCh37.p13 chr6|NW_003871062.1: 84,775-210,925 , GRCh37.p13 chr6: 112,408,456-112,534,605 LAMA4, FAM229B, 3 more genes
    nsv6799356copy number variation1nstd229human GRCh38 chr6: 112,102,221-112,140,571 , GRCh37.p13 chr6: 112,423,424-112,461,773 , GRCh37.p13 chr6|NW_003871062.1: 99,743-138,092 FAM229B, LOC107986633, 1 more genes
    nsv6619658copy number variation1nstd223human GRCh38 chr6: 112,101,413-112,103,231 , GRCh37.p13 chr6|NW_003871062.1: 98,935-100,753 , GRCh37.p13 chr6: 112,422,616-112,424,434 FAM229B
    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
    nsv6604986copy number variation1nstd223human GRCh38 chr6: 112,099,707-112,103,040 , GRCh37.p13 chr6: 112,420,910-112,424,243 , GRCh37.p13 chr6|NW_003871062.1: 97,229-100,562 FAM229B
    nsv6555692inversion1nstd223human GRCh38 chr6: 112,084,907-112,090,583 , GRCh37.p13 chr6|NW_003871062.1: 82,429-88,105 , GRCh37.p13 chr6: 112,406,110-112,411,786 FAM229B, TUBE1
    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
    nsv6313613copy number variation1nstd102humanUncertain significance GRCh37 chr6: 110,472,732-114,762,836 , GRCh38.p12 chr6: 110,151,529-114,441,672 LOC107986522, TUBE1, 87 more genes
    nsv6257034mobile element insertion1nstd215human GRCh38 chr6: 112,096,701-112,096,701 , GRCh37.p13 chr6|NW_003871062.1: 94,223-94,223 , GRCh37.p13 chr6: 112,417,904-112,417,904 FAM229B
    nsv6072107insertion1nstd212human GRCh38 chr6: 112,086,829-112,086,829 , GRCh37.p13 chr6: 112,408,032-112,408,032 , GRCh37.p13 chr6|NW_003871062.1: 84,351-84,351 TUBE1, FAM229B
    nsv5677735mobile element insertion2nstd211human GRCh38 chr6: 112,096,701-112,096,701 , GRCh37.p13 chr6: 112,417,904-112,417,904 , GRCh37.p13 chr6|NW_003871062.1: 94,223-94,223 FAM229B
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5473434copy number variation1nstd206human GRCh38 chr6: 112,101,413-112,103,231 , GRCh37.p13 chr6|NW_003871062.1: 98,935-100,753 , GRCh37.p13 chr6: 112,422,616-112,424,434 FAM229B
    nsv5412916mobile element insertion1nstd206human GRCh38 chr6: 112,096,701-112,096,732 , GRCh37.p13 chr6|NW_003871062.1: 94,223-94,254 , GRCh37.p13 chr6: 112,417,904-112,417,935 FAM229B
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