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Items: 1 to 20 of 528

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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
    nsv7145486copy number variation1nstd232human GRCh37.p13 chr18: 75,681,606-75,681,809 , GRCh38.p12 chr18: 77,969,650-77,969,853 LINC01029
    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
    nsv7076010inversion1nstd229human GRCh38 chr18: 76,851,987-80,007,706 , GRCh37.p13 chr18: 74,563,943-77,767,706 SLC66A2, CTDP1-DT, 33 more genes
    nsv7073560inversion1nstd229human GRCh38 chr18: 77,216,604-78,850,491 , GRCh37.p13 chr18: 74,928,560-76,610,491 GALR1, RNA5SP461, 10 more genes
    nsv7071334inversion1nstd229human GRCh38 chr18: 77,707,319-79,727,290 , GRCh37.p13 chr18: 75,419,275-77,487,290 RNU6-655P, LOC105372224, 20 more genes
    nsv7066896inversion1nstd229human GRCh38 chr18: 76,952,577-79,273,778 , GRCh37.p13 chr18: 74,664,533-77,033,778 LOC105372221, LOC105372224, 19 more genes
    nsv7064903inversion1nstd229human GRCh38 chr18: 77,971,567-78,085,391 , GRCh37.p13 chr18: 75,683,523-75,845,391 LINC01029, RNU6-655P
    nsv7060951inversion1nstd229human GRCh38 chr18: 76,824,737-79,967,670 , GRCh37.p13 chr18: 74,536,693-77,727,670 CTDP1-DT, KCNG2, 34 more genes
    nsv7015623copy number variation1nstd229human GRCh38 chr18: 77,170,889-80,012,828 , GRCh37.p13 chr18: 74,882,845-77,772,828 RNU6-655P, LOC107985171, 29 more genes
    nsv7014911copy number variation1nstd229human GRCh38 chr18: 77,982,001-77,991,100 , GRCh37.p13 chr18: 75,693,957-75,703,056 LINC01029
    nsv7014686copy number variation1nstd229human GRCh38 chr18: 77,992,351-77,996,703 , GRCh37.p13 chr18: 75,704,307-75,708,659 LINC01029
    nsv7013671copy number variation1nstd229human GRCh38 chr18: 77,564,359-78,799,953 , GRCh37.p13 chr18: 75,276,315-76,559,953 LOC105372221, LINC01029, 7 more genes
    nsv7007031copy number variation1nstd229human GRCh38 chr18: 77,993,125-77,994,058 , GRCh37.p13 chr18: 75,705,081-75,706,014 LINC01029
    nsv7004207copy number variation1nstd229human GRCh38 chr18: 77,635,799-79,710,878 , GRCh37.p13 chr18: 75,347,755-77,470,878 RNA5SP461, SALL3, 20 more genes
    nsv7003776copy number variation1nstd229human GRCh38 chr18: 77,971,501-78,069,800 , GRCh37.p13 chr18: 75,683,457-75,829,800 LINC01029, RNU6-655P
    nsv7003254copy number variation1nstd229human GRCh38 chr18: 77,957,701-78,044,100 , GRCh37.p13 chr18: 75,669,657-75,804,100 RNU6-655P, LINC01029
    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
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