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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7137114copy number variation1nstd102humanPathogenic GRCh37 chr15: 98,996,113-101,211,899 , GRCh38.p12 chr15: 98,452,884-100,671,694 PGPEP1L, LOC105371017, 36 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7074837inversion1nstd229human GRCh38 chr15: 98,618,777-101,109,346 , GRCh37.p13 chr15: 99,162,006-101,649,551 LOC440313, PRKXP1, 42 more genes
    nsv7065226inversion1nstd229human GRCh38 chr15: 98,338,625-100,843,802 , GRCh37.p13 chr15: 98,881,854-101,384,007 LOC102723335, LUNAR1, 39 more genes
    nsv7064824inversion1nstd229human GRCh38 chr15: 98,981,210-99,387,289 , GRCh37.p13 chr15: 99,524,439-99,927,494 SYNM-AS1, TTC23, 6 more genes
    nsv7063694inversion1nstd229human GRCh38 chr15: 98,738,473-100,284,229 , GRCh37.p13 chr15: 99,281,702-100,824,434 MIR4714, PGPEP1L, 22 more genes
    nsv7058435inversion1nstd229human GRCh38 chr15: 99,189,235-99,257,521 , GRCh37.p13 chr15: 99,729,440-99,797,726 HSP90B2P, TTC23, 1 more genes
    nsv6977420copy number variation1nstd229human GRCh38 chr15: 99,228,901-99,260,000 , GRCh37.p13 chr15: 99,769,106-99,800,205 HSP90B2P, LRRC28, 1 more genes
    nsv6977137copy number variation1nstd229human GRCh38 chr15: 98,919,969-99,497,854 , GRCh37.p13 chr15: 99,463,198-100,038,059 SYNM, LINC02244, 11 more genes
    nsv6976840copy number variation1nstd229human GRCh38 chr15: 99,204,704-99,306,705 , GRCh37.p13 chr15: 99,744,909-99,846,910 HNRNPA1P62, TTC23, 2 more genes
    nsv6969669copy number variation1nstd229human GRCh38 chr15: 99,072,984-99,466,581 , GRCh37.p13 chr15: 99,696,046-100,006,786 SYNM-AS1, TTC23, 6 more genes
    nsv6969009copy number variation1nstd229human GRCh38 chr15: 99,181,127-99,515,004 , GRCh37.p13 chr15: 99,721,332-100,055,209 LOC107984790, LOC105371019, 6 more genes
    nsv6964306copy number variation1nstd229human GRCh38 chr15: 99,083,504-99,558,228 , GRCh37.p13 chr15: 99,696,046-100,098,433 LRRC28, LOC105371017, 9 more genes
    nsv6963195copy number variation1nstd229human GRCh38 chr15: 98,972,725-99,619,452 , GRCh37.p13 chr15: 99,515,954-100,159,657 LRRC28, LOC105371017, 12 more genes
    nsv6960547copy number variation1nstd229human GRCh38 chr15: 93,794,809-100,070,222 , GRCh37.p13 chr15: 94,338,038-100,610,427 LOC105371010, LOC105371007, 81 more genes
    nsv6959250copy number variation1nstd229human GRCh38 chr15: 99,087,345-99,266,048 , GRCh37.p13 chr15: 99,696,046-99,806,253 HSP90B2P, SYNM-AS1, 3 more genes
    nsv6959201copy number variation1nstd229human GRCh38 chr15: 98,930,010-99,483,501 , GRCh37.p13 chr15: 99,473,239-100,023,706 SYNM-AS1, PGPEP1L, 9 more genes
    nsv6637948copy number variation1nstd102humanUncertain significance GRCh37 chr15: 99,507,922-100,153,799 , GRCh38.p12 chr15: 98,964,693-99,613,594 LRRC28, PGPEP1L, 13 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
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