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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672778copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,096,088-112,105,696 , GRCh38.p12 chr11: 112,225,365-112,234,973 RPS6P16, PTS
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 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
    nsv4989302copy number variation1nstd200human GRCh38 chr11: 112,103,571-112,393,649 , GRCh37.p13 chr11: 111,974,295-112,264,372 , LINC02762, 14 more genes
    nsv4729565copy number variation1nstd102humanUncertain significance GRCh37 chr11: 111,974,627-112,188,807 , GRCh38.p12 chr11: 112,103,903-112,318,084 PTS, BCO2, 11 more genes
    nsv4683962copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,097,157-112,097,259 , GRCh38.p12 chr11: 112,226,434-112,226,536 PTS
    nsv4682086copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,097,167-112,104,278 , GRCh38.p12 chr11: 112,226,444-112,233,555 RPS6P16, PTS
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4603846copy number variation1nstd183human GRCh37 chr11: 112,096,948-112,097,258 , GRCh38.p12 chr11: 112,226,225-112,226,535 PTS
    nsv4502761mobile element insertion1nstd166human GRCh37.p13 chr11: 112,104,656-112,104,656 , GRCh38.p12 chr11: 112,233,933-112,233,933 PTS, RPS6P16
    nsv4456659copy number variation1nstd102humanUncertain significance GRCh37 chr11: 110,969,076-114,578,509 , GRCh38.p12 chr11: 111,098,352-114,707,787 RPS29P19, PPP2R1B, 95 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv4374786copy number variation1nstd173human GRCh37 chr11: 111,974,436-112,264,401 , GRCh38.p12 chr11: 112,103,712-112,393,678 , RPS6P16, 14 more genes
    nsv4208207copy number variation1nstd166human GRCh37.p13 chr11: 111,863,945-112,299,942 , GRCh38.p12 chr11: 111,993,221-112,429,219 , LOC107987164, 22 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3913577copy number variation1nstd102humanPathogenic NCBI36 chr11: 105,972,805-113,384,939 , GRCh37.p13 chr11: 106,467,595-113,879,729 , GRCh38.p12 chr11: 106,596,868-114,009,007 LAYN, DDX10, 133 more genes
    nsv3911334copy number variation1nstd102humanUncertain significance GRCh37 chr11: 111,530,104-112,126,455 , NCBI36 chr11: 111,035,314-111,631,665 , GRCh38 chr11: 111,659,380-112,255,732 HSPB2, LOC107987164, 29 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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