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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093682copy number variation1nstd102humanUncertain significance GRCh37 chr11: 30,253,450-32,460,464 , GRCh38.p12 chr11: 30,231,903-32,438,918 ARL14EP, PAX6, 28 more genes
    nsv7070141inversion1nstd229human GRCh38 chr11: 29,327,534-32,366,322 , GRCh37.p13 chr11: 29,349,081-32,387,868 PAX6, PAUPAR, 35 more genes
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 more genes
    nsv6637271copy number variation1nstd102humanUncertain significance GRCh37 chr11: 31,736,984-32,119,792 , GRCh38.p12 chr11: 31,715,436-32,098,246 LOC101928385, RCN1, 8 more genes
    nsv6309193copy number variation1nstd102humanUncertain significance GRCh37 chr11: 31,669,269-32,460,464 , GRCh38.p12 chr11: 31,647,721-32,438,918 LOC107984322, PAX6-AS1, 13 more genes
    nsv5499833copy number variation1nstd206human GRCh38 chr11: 31,402,762-32,071,010 , GRCh37.p13 chr11: 31,424,309-32,092,556 LOC107984420, DNAJC24, 8 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 more genes
    nsv4387200copy number variation1nstd173human GRCh37 chr11: 31,700,854-32,093,410 , GRCh38.p12 chr11: 31,679,306-32,071,864 ELP4, LOC101928385, 6 more genes
    nsv3922794copy number variation1nstd102humanPathogenic GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119 LOC107984419, LINC02758, 150 more genes
    nsv3922664copy number variation1nstd102humanPathogenic GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709 CSTF3, LOC101928338, 170 more genes
    nsv3922079copy number variation1nstd102humanUncertain significance GRCh38 chr11: 31,634,904-32,088,303 , GRCh37 chr11: 31,656,451-32,109,849 , NCBI36 chr11: 31,613,027-32,066,425 PAX6-AS1, ELP4, 7 more genes
    nsv3920730copy number variation1nstd102humanPathogenic GRCh38 chr11: 31,600,532-32,122,801 , GRCh37 chr11: 31,622,079-32,144,347 , NCBI36 chr11: 31,578,655-32,100,923 LOC105376613, LINC03031, 9 more genes
    nsv3917444copy number variation1nstd102humanUncertain significance NCBI36 chr11: 31,758,960-32,066,425 , GRCh37 chr11: 31,802,384-32,109,849 , GRCh38 chr11: 31,780,836-32,088,303 LOC105376613, EIF4A2P5, 7 more genes
    nsv3916247copy number variation1nstd102humanUncertain significance NCBI36 chr11: 31,698,486-32,303,638 , GRCh37 chr11: 31,741,910-32,347,062 , GRCh38 chr11: 31,720,362-32,325,516 PAUPAR, LOC107984420, 11 more genes
    nsv3912739copy number variation1nstd102humanUncertain significance GRCh37 chr11: 31,818,255-31,945,914 , NCBI36 chr11: 31,774,831-31,902,490 , GRCh38 chr11: 31,796,707-31,924,368 PAX6, PAUPAR, 1 more genes
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