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Items: 1 to 20 of 616

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094391copy number variation1nstd102humanPathogenic GRCh37 chr15: 56,961,021-57,839,688 , GRCh38.p12 chr15: 56,668,823-57,547,490 ZNF280D, LOC107984759, 11 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv6977123copy number variation1nstd229human GRCh38 chr15: 57,420,555-57,425,608 , GRCh37.p13 chr15: 57,712,753-57,717,806 CGNL1
    nsv6977122copy number variation1nstd229human GRCh38 chr15: 57,401,978-57,402,517 , GRCh37.p13 chr15: 57,694,176-57,694,715 CGNL1
    nsv6975510copy number variation1nstd229human GRCh38 chr15: 57,526,459-57,554,053 , GRCh37.p13 chr15: 57,818,657-57,846,251 CGNL1, RPS13P7
    nsv6973143copy number variation1nstd229human GRCh38 chr15: 57,368,878-57,382,286 , GRCh37.p13 chr15: 57,661,076-57,674,484 CGNL1
    nsv6973008copy number variation1nstd229human GRCh38 chr15: 57,350,452-57,488,224 , GRCh37.p13 chr15: 57,642,650-57,780,422 RNU6-844P, LOC107984759, 1 more genes
    nsv6972575copy number variation1nstd229human GRCh38 chr15: 57,380,801-57,386,100 , GRCh37.p13 chr15: 57,672,999-57,678,298 CGNL1
    nsv6971086copy number variation1nstd229human GRCh38 chr15: 57,397,494-57,399,494 , GRCh37.p13 chr15: 57,689,692-57,691,692 CGNL1
    nsv6971072copy number variation1nstd229human GRCh38 chr15: 57,481,901-57,485,700 , GRCh37.p13 chr15: 57,774,099-57,777,898 CGNL1
    nsv6971058copy number variation1nstd229human GRCh38 chr15: 57,471,636-57,473,506 , GRCh37.p13 chr15: 57,763,834-57,765,704 CGNL1
    nsv6969542copy number variation1nstd229human GRCh38 chr15: 57,462,686-57,532,425 , GRCh37.p13 chr15: 57,754,884-57,824,623 CGNL1, LOC107984759
    nsv6969292copy number variation1nstd229human GRCh38 chr15: 57,465,428-57,483,583 , GRCh37.p13 chr15: 57,757,626-57,775,781 CGNL1
    nsv6966191copy number variation1nstd229human GRCh38 chr15: 57,387,003-57,387,357 , GRCh37.p13 chr15: 57,679,201-57,679,555 CGNL1
    nsv6965980copy number variation1nstd229human GRCh38 chr15: 57,372,474-57,547,531 , GRCh37.p13 chr15: 57,664,672-57,839,729 RNU6-844P, LOC107984759, 1 more genes
    nsv6965350copy number variation1nstd229human GRCh38 chr15: 57,535,801-57,562,000 , GRCh37.p13 chr15: 57,827,999-57,854,198 RPS13P7, CGNL1
    nsv6963332copy number variation1nstd229human GRCh38 chr15: 57,526,009-57,699,984 , GRCh37.p13 chr15: 57,818,207-57,992,182 RPS13P7, CGNL1, 2 more genes
    nsv6963048copy number variation1nstd229human GRCh38 chr15: 57,399,312-57,435,833 , GRCh37.p13 chr15: 57,691,510-57,728,031 CGNL1, RNU6-844P
    nsv6961903copy number variation1nstd229human GRCh38 chr15: 57,487,576-57,507,302 , GRCh37.p13 chr15: 57,779,774-57,799,500 CGNL1, LOC107984759
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