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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147196copy number variation1nstd232human GRCh37.p13 chr11: 124,830,138-124,830,245 , GRCh38.p12 chr11: 124,960,242-124,960,349 CCDC15
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6916077copy number variation1nstd229human GRCh38 chr11: 124,575,701-124,974,400 , GRCh37.p13 chr11: 124,445,597-124,844,296 SIAE, HEPACAM, 19 more genes
    nsv6912865copy number variation1nstd229human GRCh38 chr11: 125,025,695-125,029,272 , GRCh37.p13 chr11: 124,895,591-124,899,168 CCDC15
    nsv6911672copy number variation1nstd229human GRCh38 chr11: 125,021,501-125,027,400 , GRCh37.p13 chr11: 124,891,397-124,897,296 CCDC15
    nsv6908948copy number variation1nstd229human GRCh38 chr11: 124,964,175-124,970,974 , GRCh37.p13 chr11: 124,834,071-124,840,870 CCDC15
    nsv6907456copy number variation1nstd229human GRCh38 chr11: 125,002,929-125,019,478 , GRCh37.p13 chr11: 124,872,825-124,889,374 CCDC15
    nsv6907395copy number variation1nstd229human GRCh38 chr11: 125,026,496-125,038,381 , GRCh37.p13 chr11: 124,896,392-124,908,277 CCDC15
    nsv6905529copy number variation1nstd229human GRCh38 chr11: 124,965,714-124,977,620 , GRCh37.p13 chr11: 124,835,610-124,847,516 CCDC15
    nsv6904587copy number variation1nstd229human GRCh38 chr11: 124,957,622-124,960,755 , GRCh37.p13 chr11: 124,827,518-124,830,651 CCDC15
    nsv6903595copy number variation1nstd229human GRCh38 chr11: 125,025,701-125,029,300 , GRCh37.p13 chr11: 124,895,597-124,899,196 CCDC15
    nsv6902979copy number variation1nstd229human GRCh38 chr11: 124,957,740-124,984,047 , GRCh37.p13 chr11: 124,827,636-124,853,943 CCDC15
    nsv6902461copy number variation1nstd229human GRCh38 chr11: 124,988,557-124,988,708 , GRCh37.p13 chr11: 124,858,453-124,858,604 CCDC15
    nsv6902346copy number variation1nstd229human GRCh38 chr11: 124,949,193-124,952,898 , GRCh37.p13 chr11: 124,819,089-124,822,794 CCDC15, CCDC15-DT
    nsv6902000copy number variation1nstd229human GRCh38 chr11: 125,018,718-125,023,109 , GRCh37.p13 chr11: 124,888,614-124,893,005 CCDC15
    nsv6637933copy number variation1nstd102humanUncertain significance GRCh37 chr11: 124,788,547-124,894,689 , GRCh38.p12 chr11: 124,918,651-125,024,793 HEPN1, HEPACAM, 3 more genes
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6466371copy number variation1nstd223human GRCh38 chr11: 125,010,097-125,011,265 , GRCh37.p13 chr11: 124,879,993-124,881,161 CCDC15
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