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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6977555copy number variation1nstd229human GRCh38 chr15: 40,378,801-40,382,100 , GRCh37.p13 chr15: 40,671,002-40,674,301 DISP2, KNSTRN
    nsv6976300copy number variation1nstd229human GRCh38 chr15: 40,335,825-40,358,076 , GRCh37.p13 chr15: 40,628,026-40,650,277 CCDC9B, DISP2, 1 more genes
    nsv6975647copy number variation1nstd229human GRCh38 chr15: 40,349,499-40,354,622 , GRCh37.p13 chr15: 40,641,700-40,646,823 PHGR1, DISP2
    nsv6969050copy number variation1nstd229human GRCh38 chr15: 40,229,801-40,497,200 , GRCh37.p13 chr15: 40,522,002-40,789,399 CCDC9B, KNSTRN, 16 more genes
    nsv6964883copy number variation1nstd229human GRCh38 chr15: 39,883,301-41,010,600 , GRCh37.p13 chr15: 40,175,502-41,302,798 SRP14, BUB1B-PAK6, 54 more genes
    nsv6963530copy number variation1nstd229human GRCh38 chr15: 40,357,471-40,357,507 , GRCh37.p13 chr15: 40,649,672-40,649,708 DISP2
    nsv6958687copy number variation1nstd229human GRCh38 chr15: 40,349,891-40,353,968 , GRCh37.p13 chr15: 40,642,092-40,646,169 DISP2, PHGR1
    nsv6498869copy number variation1nstd223human GRCh38 chr15: 40,352,069-40,352,747 , GRCh37.p13 chr15: 40,644,270-40,644,948 PHGR1, DISP2
    nsv6241963mobile element insertion1nstd215human GRCh38 chr15: 40,374,571-40,374,571 , GRCh37.p13 chr15: 40,666,772-40,666,772 DISP2
    nsv6132806copy number variation1nstd213human GRCh37 chr15: 39,170,000-42,090,001 , GRCh38.p12 chr15: 38,877,799-41,797,803 GCHFR, LTK, 84 more genes
    nsv6113876mobile element insertion1nstd186human GRCh37 chr15: 40,666,772-40,666,809 , GRCh38.p12 chr15: 40,374,571-40,374,608 DISP2
    nsv6099963insertion1nstd212human GRCh38 chr15: 40,374,014-40,374,014 , GRCh37.p13 chr15: 40,666,215-40,666,215 DISP2
    nsv6081492insertion1nstd212human GRCh38 chr15: 40,374,556-40,374,556 , GRCh37.p13 chr15: 40,666,757-40,666,757 DISP2
    nsv6021022copy number variation1nstd212human GRCh38 chr15: 40,356,156-40,356,218 , GRCh37.p13 chr15: 40,648,357-40,648,419 DISP2, PHGR1
    nsv5968500insertion1nstd209human GRCh38 chr15: 40,374,556-40,374,556 , GRCh37.p13 chr15: 40,666,757-40,666,757 DISP2
    nsv5928387copy number variation1nstd209human GRCh38 chr15: 40,356,113-40,356,244 , GRCh37.p13 chr15: 40,648,314-40,648,445 DISP2, PHGR1
    nsv5719722mobile element insertion1nstd211human GRCh38 chr15: 40,355,519-40,355,519 , GRCh37.p13 chr15: 40,647,720-40,647,720 DISP2, PHGR1
    nsv5669729inversion1nstd207human GRCh38 chr15: 40,333,147-40,369,327 , GRCh37.p13 chr15: 40,625,348-40,661,528 DISP2, CCDC9B, 1 more genes
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