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Items: 1 to 20 of 396

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7137137copy number variation1nstd102humanPathogenic GRCh37 chr18: 71,740,696-78,005,231 , GRCh38.p12 chr18: 74,073,461-80,247,348 LOC339298, LOC105372201, 84 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7072337inversion1nstd229human GRCh38 chr18: 76,848,310-76,848,327 , GRCh37.p13 chr18: 74,560,266-74,560,283 ZNF236, LOC105372214
    nsv7060951inversion1nstd229human GRCh38 chr18: 76,824,737-79,967,670 , GRCh37.p13 chr18: 74,536,693-77,727,670 CTDP1-DT, KCNG2, 34 more genes
    nsv7015592copy number variation1nstd229human GRCh38 chr18: 76,497,101-76,900,200 , GRCh37.p13 chr18: 74,209,058-74,612,156 LOC107985151, RNU6-346P, 14 more genes
    nsv7004307copy number variation1nstd229human GRCh38 chr18: 76,563,291-76,861,516 , GRCh37.p13 chr18: 74,275,248-74,573,472 LINC00683, LOC105372212, 11 more genes
    nsv6638045copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240 LOC105372211, LOC105372188, 128 more genes
    nsv6638004copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,520,071-78,014,123 , GRCh38.p12 chr18: 63,852,837-80,256,240 LOC107985151, CD226, 165 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
    nsv6634444copy number variation1nstd102humanPathogenic GRCh37 chr18: 72,669,936-77,889,946 , GRCh38.p12 chr18: 74,957,980-80,132,063 LOC105372212, GALR1, 71 more genes
    nsv6599107inversion1nstd223human GRCh38 chr18: 76,840,428-76,841,131 , GRCh37.p13 chr18: 74,552,384-74,553,087 LOC105372214, ZNF236
    nsv6531635copy number variation1nstd223human GRCh38 chr18: 76,843,473-76,845,554 , GRCh37.p13 chr18: 74,555,429-74,557,510 LOC105372214, ZNF236
    nsv6530519copy number variation1nstd223human GRCh38 chr18: 76,846,874-76,847,519 , GRCh37.p13 chr18: 74,558,830-74,559,475 LOC105372214, ZNF236
    nsv6526899copy number variation1nstd223human GRCh38 chr18: 76,837,061-76,841,111 , GRCh37.p13 chr18: 74,549,017-74,553,067 LOC105372214, ZNF236
    nsv6521965copy number variation1nstd223human GRCh38 chr18: 76,844,584-76,848,043 , GRCh37.p13 chr18: 74,556,540-74,559,999 LOC105372214, ZNF236
    nsv6521035copy number variation1nstd223human GRCh38 chr18: 76,563,291-76,861,516 , GRCh37.p13 chr18: 74,275,248-74,573,472 LINC01927, CCND3P2, 11 more genes
    nsv6518953copy number variation1nstd223human GRCh38 chr18: 76,664,424-76,847,645 , GRCh37.p13 chr18: 74,376,381-74,559,601 LOC105372212, CCND3P2, 8 more genes
    nsv6315531copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,289,055-78,014,123 , GRCh38.p12 chr18: 63,621,821-80,256,240 RN7SL795P, ZNF407, 169 more genes
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