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Items: 1 to 20 of 28

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3899890copy number variation1nstd102humanBenign GRCh37 chr11: 102,922,881-103,203,377 , GRCh38.p12 chr11: 103,052,152-103,332,649 DCUN1D5, DYNC2H1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 DCUN1D5, FAUP4, 2031 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 DCUN1D5, RPS6P16, 449 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 DCUN1D5, PLS1P1, 349 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 DCUN1D5, PHB1P16, 385 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 DCUN1D5, LOC107984375, 295 more genes
    nsv3894488copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924 DCUN1D5, RNU6-16P, 270 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 DCUN1D5, LOC101060084, 230 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 DCUN1D5, HSPD1P13, 239 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 DCUN1D5, GRIA4, 111 more genes
    nsv3924464copy number variation1nstd102humanPathogenic NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873 DCUN1D5, ARHGAP42, 91 more genes
    nsv6309019copy number variation2nstd102humanPathogenic GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253 DCUN1D5, RPL21P96, 40 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 DCUN1D5, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 DCUN1D5, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 DCUN1D5, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 DCUN1D5, PYGM, 2125 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 DCUN1D5, SESN3, 694 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 DCUN1D5, RPS27P19, 655 more genes
    nsv3915056copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,323,715-103,914,833 , NCBI36 chr11: 100,828,925-103,420,043 , GRCh38 chr11: 101,452,984-104,044,105 DCUN1D5, MMP27, 47 more genes
    nsv3890271copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 98,515,900-104,970,876 , GRCh38.p12 chr11: 98,645,170-105,100,149 DCUN1D5, BIRC2, 78 more genes
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