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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7070377inversion1nstd229human GRCh38 chr11: 112,386,733-113,822,442 , GRCh37.p13 chr11: 112,257,456-113,693,164 RPS29P19, ZW10, 25 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv7065476inversion1nstd229human GRCh38 chr11: 112,386,765-113,815,738 , GRCh37.p13 chr11: 112,257,488-113,686,460 TTC12, RPL23AP62, 24 more genes
    nsv6917882copy number variation1nstd229human GRCh38 chr11: 113,309,391-113,326,316 , GRCh37.p13 chr11|NW_003871078.1: 492,117-509,042 , GRCh37.p13 chr11: 113,180,113-113,197,038 TTC12
    nsv6914286copy number variation1nstd229human GRCh38 chr11: 113,330,481-113,333,172 , GRCh37.p13 chr11|NW_003871078.1: 513,207-515,898 , GRCh37.p13 chr11: 113,201,203-113,203,894 TTC12
    nsv6913981copy number variation1nstd229human GRCh38 chr11: 113,310,912-113,314,118 , GRCh37.p13 chr11: 113,181,634-113,184,840 , GRCh37.p13 chr11|NW_003871078.1: 493,638-496,844 TTC12
    nsv6911790copy number variation1nstd229human GRCh38 chr11: 113,328,487-113,333,259 , GRCh37.p13 chr11|NW_003871078.1: 511,213-515,985 , GRCh37.p13 chr11: 113,199,209-113,203,981 TTC12
    nsv6905338copy number variation1nstd229human GRCh38 chr11: 113,303,622-113,401,455 , GRCh37.p13 chr11|NW_003871078.1: 486,348-546,435 , GRCh37.p13 chr11: 113,174,344-113,234,431 TTC12, ANKK1
    nsv6905192copy number variation1nstd229human GRCh38 chr11: 113,336,128-113,336,325 , GRCh37.p13 chr11: 113,206,850-113,207,047 , GRCh37.p13 chr11|NW_003871078.1: 518,854-519,051 TTC12
    nsv6904207copy number variation1nstd229human GRCh38 chr11: 113,319,036-113,323,257 , GRCh37.p13 chr11: 113,189,758-113,193,979 , GRCh37.p13 chr11|NW_003871078.1: 501,762-505,983 TTC12
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6462376copy number variation1nstd223human GRCh38 chr11: 113,349,659-113,351,497 , GRCh37.p13 chr11: 113,220,381-113,222,219 , GRCh37.p13 chr11|NW_003871078.1: 532,385-534,223 TTC12
    nsv6460526copy number variation1nstd223human GRCh38 chr11: 113,357,601-113,359,900 , GRCh37.p13 chr11: 113,228,323-113,230,622 , GRCh37.p13 chr11|NW_003871078.1: 540,327-542,626 TTC12
    nsv6458250copy number variation1nstd223human GRCh38 chr11: 113,334,347-113,334,911 , GRCh37.p13 chr11: 113,205,069-113,205,633 , GRCh37.p13 chr11|NW_003871078.1: 517,073-517,637 TTC12
    nsv6457451copy number variation1nstd223human GRCh38 chr11: 113,341,453-113,341,972 , GRCh37.p13 chr11|NW_003871078.1: 524,179-524,698 , GRCh37.p13 chr11: 113,212,175-113,212,694 TTC12
    nsv6456054copy number variation1nstd223human GRCh38 chr11: 113,335,001-113,338,400 , GRCh37.p13 chr11|NW_003871078.1: 517,727-521,126 , GRCh37.p13 chr11: 113,205,723-113,209,122 TTC12
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
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