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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7146078copy number variation1nstd232human GRCh37.p13 chr7: 154,738,297-154,738,387 , GRCh38.p12 chr7: 154,946,587-154,946,677 PAXIP1, PAXIP1-AS2
    nsv7137106copy number variation1nstd102humanUncertain significance GRCh37 chr7: 154,633,174-155,446,847 , GRCh38.p12 chr7: 154,841,464-155,654,153 RBM33, RBM33-DT, 21 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv7068159inversion1nstd229human GRCh38 chr7: 154,965,127-154,977,032 , GRCh37.p13 chr7: 154,756,837-154,768,742 PAXIP1
    nsv7066063inversion1nstd229human GRCh38 chr7: 154,951,832-155,229,069 , GRCh37.p13 chr7: 154,743,542-155,020,779 RN7SKP280, PAXIP1, 4 more genes
    nsv7064384inversion1nstd229human GRCh38 chr7: 154,947,117-154,960,749 , GRCh37.p13 chr7: 154,738,827-154,752,459 PAXIP1-AS2, PAXIP1
    nsv7059819inversion1nstd229human GRCh38 chr7: 154,946,883-154,950,349 , GRCh37.p13 chr7: 154,738,593-154,742,059 PAXIP1, PAXIP1-AS2
    nsv7058470inversion1nstd229human GRCh38 chr7: 154,978,887-154,981,095 , GRCh37.p13 chr7: 154,770,597-154,772,805 PAXIP1
    nsv6834022copy number variation1nstd229human GRCh38 chr7: 154,808,210-155,712,129 , GRCh37.p13 chr7: 154,599,920-155,504,823 RBM33, LOC105375594, 21 more genes
    nsv6831908copy number variation1nstd229human GRCh38 chr7: 154,786,490-155,280,606 , GRCh37.p13 chr7: 154,578,200-155,072,316 RN7SKP280, DPP6, 10 more genes
    nsv6830108copy number variation1nstd229human GRCh38 chr7: 154,977,924-154,977,955 , GRCh37.p13 chr7: 154,769,634-154,769,665 PAXIP1
    nsv6827088copy number variation1nstd229human GRCh38 chr7: 154,977,915-154,977,981 , GRCh37.p13 chr7: 154,769,625-154,769,691 PAXIP1
    nsv6826352copy number variation1nstd229human GRCh38 chr7: 154,829,601-154,951,800 , GRCh37.p13 chr7: 154,621,311-154,743,510 DPP6, LOC105375580, 2 more genes
    nsv6824525copy number variation1nstd229human GRCh38 chr7: 152,687,878-156,500,924 , GRCh37.p13 chr7: 152,384,963-156,293,618 RN7SKP280, LINC03010, 44 more genes
    nsv6820929copy number variation1nstd229human GRCh38 chr7: 154,988,601-154,992,300 , GRCh37.p13 chr7: 154,780,311-154,784,010 PAXIP1
    nsv6819682copy number variation1nstd229human GRCh38 chr7: 154,994,739-154,994,938 , GRCh37.p13 chr7: 154,786,449-154,786,648 PAXIP1
    nsv6818641copy number variation1nstd229human GRCh38 chr7: 154,971,520-154,974,769 , GRCh37.p13 chr7: 154,763,230-154,766,479 PAXIP1
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