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Items: 1 to 20 of 678

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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
    nsv7071177inversion1nstd229human GRCh38 chr11: 113,105,983-113,106,001 , GRCh37.p13 chr11: 112,976,705-112,976,723 , GRCh37.p13 chr11|NW_003871078.1: 288,709-288,727 NCAM1
    nsv7071064inversion1nstd229human GRCh38 chr11: 113,144,287-113,144,815 , GRCh37.p13 chr11|NW_003871078.1: 327,013-327,541 , GRCh37.p13 chr11: 113,015,009-113,015,537 NCAM1
    nsv7070493inversion1nstd229human GRCh38 chr11: 112,973,984-112,998,409 , GRCh37.p13 chr11|NW_003871078.1: 156,710-181,135 , GRCh37.p13 chr11: 112,844,706-112,869,131 NCAM1, RNU7-187P
    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
    nsv7063579inversion1nstd229human GRCh38 chr11: 113,057,684-113,057,718 , GRCh37.p13 chr11: 112,928,406-112,928,440 , GRCh37.p13 chr11|NW_003871078.1: 240,410-240,444 NCAM1
    nsv6918011copy number variation1nstd229human GRCh38 chr11: 112,989,948-112,992,634 , GRCh37.p13 chr11|NW_003871078.1: 172,674-175,360 , GRCh37.p13 chr11: 112,860,670-112,863,356 NCAM1
    nsv6917844copy number variation1nstd229human GRCh38 chr11: 113,093,809-113,097,299 , GRCh37.p13 chr11: 112,964,531-112,968,021 , GRCh37.p13 chr11|NW_003871078.1: 276,535-280,025 NCAM1
    nsv6917363copy number variation1nstd229human GRCh38 chr11: 113,086,308-113,090,815 , GRCh37.p13 chr11: 112,957,030-112,961,537 , GRCh37.p13 chr11|NW_003871078.1: 269,034-273,541 NCAM1
    nsv6915510copy number variation1nstd229human GRCh38 chr11: 112,980,154-112,994,836 , GRCh37.p13 chr11: 112,850,876-112,865,558 , GRCh37.p13 chr11|NW_003871078.1: 162,880-177,562 NCAM1
    nsv6915081copy number variation1nstd229human GRCh38 chr11: 113,140,908-113,144,814 , GRCh37.p13 chr11: 113,011,630-113,015,536 , GRCh37.p13 chr11|NW_003871078.1: 323,634-327,540 NCAM1
    nsv6914770copy number variation1nstd229human GRCh38 chr11: 113,008,601-113,012,100 , GRCh37.p13 chr11: 112,879,323-112,882,822 , GRCh37.p13 chr11|NW_003871078.1: 191,327-194,826 NCAM1
    nsv6914374copy number variation1nstd229human GRCh38 chr11: 113,158,501-113,195,684 , GRCh37.p13 chr11|NW_003871078.1: 341,227-378,410 , GRCh37.p13 chr11: 113,029,223-113,066,406 NCAM1
    nsv6913302copy number variation1nstd229human GRCh38 chr11: 113,223,601-113,230,800 , GRCh37.p13 chr11: 113,094,323-113,101,522 , GRCh37.p13 chr11|NW_003871078.1: 406,327-413,526 NCAM1
    nsv6911674copy number variation1nstd229human GRCh38 chr11: 113,055,990-113,077,604 , GRCh37.p13 chr11: 112,926,712-112,948,326 , GRCh37.p13 chr11|NW_003871078.1: 238,716-260,330 NCAM1
    nsv6910960copy number variation1nstd229human GRCh38 chr11: 113,177,149-113,180,175 , GRCh37.p13 chr11: 113,047,871-113,050,897 , GRCh37.p13 chr11|NW_003871078.1: 359,875-362,901 NCAM1
    nsv6910867copy number variation1nstd229human GRCh38 chr11: 113,115,501-113,119,100 , GRCh37.p13 chr11: 112,986,223-112,989,822 , GRCh37.p13 chr11|NW_003871078.1: 298,227-301,826 NCAM1
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