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Items: 1 to 20 of 487

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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
    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
    nsv7014599copy number variation1nstd229human GRCh38 chr18: 76,635,239-76,636,040 , GRCh37.p13 chr18: 74,347,196-74,347,997 LINC01927
    nsv7006812copy number variation1nstd229human GRCh38 chr18: 76,615,992-76,621,736 , GRCh37.p13 chr18: 74,327,949-74,333,693 LINC00683, LINC01927
    nsv7006696copy number variation1nstd229human GRCh38 chr18: 76,607,833-76,725,498 , GRCh37.p13 chr18: 74,319,790-74,437,454 LINC00683, LINC01879, 5 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
    nsv7002985copy number variation1nstd229human GRCh38 chr18: 76,628,101-76,631,800 , GRCh37.p13 chr18: 74,340,058-74,343,757 LINC01927
    nsv7002871copy number variation1nstd229human GRCh38 chr18: 76,564,502-76,631,865 , GRCh37.p13 chr18: 74,276,459-74,343,822 LINC00683, LINC01927
    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
    nsv6637395copy number variation1nstd102humanUncertain significance GRCh37 chr18: 73,711,236-74,360,445 , GRCh38.p12 chr18: 75,999,281-76,648,488 LOC105372204, LOC339298, 12 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
    nsv6595969inversion1nstd223human GRCh38 chr18: 76,630,471-76,631,277 , GRCh37.p13 chr18: 74,342,428-74,343,234 LINC01927
    nsv6532298copy number variation1nstd223human GRCh38 chr18: 76,625,153-76,626,014 , GRCh37.p13 chr18: 74,337,110-74,337,971 LINC01927
    nsv6527991copy number variation1nstd223human GRCh38 chr18: 76,639,491-76,641,706 , GRCh37.p13 chr18: 74,351,448-74,353,663 LINC01927
    nsv6526728copy number variation1nstd223human GRCh38 chr18: 76,614,513-76,681,305 , GRCh37.p13 chr18: 74,326,470-74,393,262 LOC105372212, LINC01927, 2 more genes
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