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Items: 1 to 20 of 112

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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
    nsv7070958inversion1nstd229human GRCh38 chr11: 29,042,371-30,786,159 , GRCh37.p13 chr11: 29,063,918-30,807,706 LOC100421558, LINC02546, 18 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
    nsv6901489copy number variation1nstd229human GRCh38 chr11: 29,922,234-30,610,383 , GRCh37.p13 chr11: 29,943,781-30,631,930 KCNA4, FSHB, 8 more genes
    nsv6591112inversion1nstd223human GRCh38 chr11: 30,327,935-30,328,154 , GRCh37.p13 chr11: 30,349,482-30,349,701 ARL14EP
    nsv6450291copy number variation1nstd223human GRCh38 chr11: 30,119,133-31,636,993 , GRCh37.p13 chr11: 30,140,680-31,658,540 RPL12P30, LOC105376611, 14 more genes
    nsv6439962copy number variation1nstd223human GRCh38 chr11: 30,321,025-30,334,443 , GRCh37.p13 chr11: 30,342,572-30,355,990 ARL14EP-DT, ARL14EP
    nsv6436741copy number variation1nstd223human GRCh38 chr11: 30,320,690-30,321,452 , GRCh37.p13 chr11: 30,342,237-30,342,999 ARL14EP, ARL14EP-DT
    nsv6315083copy number variation1nstd102humannot provided GRCh37 chr11: 27,547,893-31,656,604 , GRCh38.p12 chr11: 27,526,346-31,635,057 KIF18A, ARL14EP-DT, 41 more genes
    nsv5976171insertion1nstd209human GRCh38 chr11: 30,334,208-30,334,208 , GRCh37.p13 chr11: 30,355,755-30,355,755 ARL14EP
    nsv5925977copy number variation1nstd209human GRCh38 chr11: 30,336,473-30,336,526 , GRCh37.p13 chr11: 30,358,020-30,358,073 ARL14EP
    nsv5847720copy number variation1nstd209human GRCh38 chr11: 30,318,105-30,321,370 , GRCh37.p13 chr11: 30,339,652-30,342,917 ARL14EP-DT, ARL14EP
    nsv5503134copy number variation1nstd206human GRCh38 chr11: 30,330,094-30,330,344 , GRCh37.p13 chr11: 30,351,641-30,351,891 ARL14EP
    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
    nsv3939995insertion1nstd167human GRCh37 chr11: 30,355,755-30,355,755 , GRCh38.p12 chr11: 30,334,208-30,334,208 ARL14EP
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