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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7073567inversion1nstd229human GRCh38 chr11: 73,812,649-75,298,624 , GRCh37.p13 chr11: 73,523,694-75,009,668 LIPT2, RNF169, 51 more genes
    nsv7073187inversion1nstd229human GRCh38 chr11: 74,758,590-74,858,901 , GRCh37.p13 chr11: 74,469,635-74,569,946 XRRA1, RNF169, 1 more genes
    nsv6917616copy number variation1nstd229human GRCh38 chr11: 74,806,696-74,807,068 , GRCh37.p13 chr11: 74,517,741-74,518,113 RNF169
    nsv6915516copy number variation1nstd229human GRCh38 chr11: 74,807,801-74,815,700 , GRCh37.p13 chr11: 74,518,846-74,526,745 RNF169
    nsv6914527copy number variation1nstd229human GRCh38 chr11: 74,812,000-74,812,641 , GRCh37.p13 chr11: 74,523,045-74,523,686 RNF169
    nsv6911422copy number variation1nstd229human GRCh38 chr11: 74,750,207-74,758,690 , GRCh37.p13 chr11: 74,461,252-74,469,735 RNF169
    nsv6906106copy number variation1nstd229human GRCh38 chr11: 74,821,378-74,821,678 , GRCh37.p13 chr11: 74,532,423-74,532,723 RNF169
    nsv6906019copy number variation1nstd229human GRCh38 chr11: 74,779,277-74,783,085 , GRCh37.p13 chr11: 74,490,322-74,494,130 RNF169
    nsv6904026copy number variation1nstd229human GRCh38 chr11: 74,791,892-74,792,078 , GRCh37.p13 chr11: 74,502,937-74,503,123 RNF169
    nsv6903484copy number variation1nstd229human GRCh38 chr11: 74,806,023-74,806,091 , GRCh37.p13 chr11: 74,517,068-74,517,136 RNF169
    nsv6901750copy number variation1nstd229human GRCh38 chr11: 74,827,960-74,830,930 , GRCh37.p13 chr11: 74,539,005-74,541,975 RNF169
    nsv6901355copy number variation1nstd229human GRCh38 chr11: 74,780,695-74,793,282 , GRCh37.p13 chr11: 74,491,740-74,504,327 RNF169
    nsv6901290copy number variation1nstd229human GRCh38 chr11: 74,822,164-74,823,070 , GRCh37.p13 chr11: 74,533,209-74,534,115 RNF169
    nsv6590993inversion1nstd223human GRCh38 chr11: 74,527,351-75,035,337 , GRCh37.p13 chr11: 74,238,396-74,746,382 CHRDL2, RPS12P22, 14 more genes
    nsv6588054inversion1nstd223human GRCh38 chr11: 74,794,987-74,795,699 , GRCh37.p13 chr11: 74,506,032-74,506,744 RNF169
    nsv6585665inversion1nstd223human GRCh38 chr11: 74,750,882-74,752,009 , GRCh37.p13 chr11: 74,461,927-74,463,054 RNF169
    nsv6585166inversion1nstd223human GRCh38 chr11: 74,813,864-74,814,103 , GRCh37.p13 chr11: 74,524,909-74,525,148 RNF169
    nsv6582924inversion1nstd223human GRCh38 chr11: 74,767,556-74,768,326 , GRCh37.p13 chr11: 74,478,601-74,479,371 RNF169
    nsv6582009inversion1nstd223human GRCh38 chr11: 74,802,651-74,803,109 , GRCh37.p13 chr11: 74,513,696-74,514,154 RNF169
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