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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3962548insertion1nstd168human GRCh38 (hg38) chr11: 102,700,540-102,745,926 , GRCh37.p13 chr11: 102,571,271-102,616,657 MMP8, MMP27
    nsv3924464copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr11: 98,357,901-106,059,146 , GRCh37.p13 chr11: 98,228,629-105,929,873 , NCBI36 (hg18) chr11: 97,733,839-105,435,083 BIRC3, CASP1, 92 more genes
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr11: 85,242,847-102,920,097 , GRCh37.p13 chr11: 84,953,891-102,702,496 , NCBI36 (hg18) chr11: 84,631,539-102,296,037 BIRC3, CTSC, 245 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr11: 100,348,599-135,040,246 , GRCh37.p13 chr11: 100,219,331-134,910,140 , NCBI36 (hg18) chr11: 99,724,541-134,415,350 ACRV1, BIRC2, 675 more genes
    nsv3915056copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr11: 101,452,984-104,044,105 , GRCh37.p13 chr11: 101,323,715-103,914,833 , NCBI36 (hg18) chr11: 100,828,925-103,420,043 MMP1, MMP10, 47 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr11: 78,232,836-106,779,420 , GRCh37.p13 chr11: 77,943,882-106,650,146 , NCBI36 (hg18) chr11: 77,621,530-106,155,356 BIRC3, CASP1, 356 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr11: 91,086,659-109,595,582 , GRCh37.p13 chr11: 90,819,827-109,466,308 , NCBI36 (hg18) chr11: 90,459,475-108,971,518 BIRC3, CASP1, 233 more genes
    nsv3910387copy number variation1nstd102humanLikely benign NCBI36 (hg18) chr11: 101,948,892-102,308,304 , GRCh37.p13 chr11: 102,443,682-102,738,968 , GRCh38.p12 chr11: 102,572,951-102,932,365 MMP10, MMP27, 11 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 (hg18) 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 BIRC2, DDX10, 394 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 , NCBI36 (hg18) chr11: 220,616-134,443,680 ACAT1, ACTN3, 2901 more genes
    nsv3908142copy number variation1nstd102humanLikely pathogenic GRCh37 (hg19) chr11: 102,578,709-107,230,611 , GRCh38.p12 chr11: 102,707,978-107,359,885 , NCBI36 (hg18) chr11: 102,083,919-106,735,821 MMP1, MMP10, 65 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 , NCBI36 (hg18) chr11: 79,731,102-112,821,446 FDX1, FUT4, 460 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 , NCBI36 (hg18) chr11: 188,510-134,439,273 ACRV1, ADM, 2905 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 , NCBI36 (hg18) chr11: 71,266,453-116,186,128 ARRB1, ART2P, 713 more genes
    nsv3894488copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924 , NCBI36 (hg18) chr11: 87,792,106-108,919,860 ACAT1, BIRC3, 275 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 , NCBI36 (hg18) chr11: 60,864-134,443,680 ACAT1, ALDH3B1, 2915 more genes
    nsv3890271copy number variation1nstd102humanLikely pathogenic GRCh37 (hg19) chr11: 98,515,900-104,970,876 , GRCh38.p12 chr11: 98,645,170-105,100,149 , NCBI36 (hg18) chr11: 98,021,110-104,476,086 CASP5, MMP1, 79 more genes
    nsv3558284sequence alteration2nstd152human GRCh38 (hg38) chr11: 102,719,412-102,720,554 , GRCh37.p13 chr11: 102,590,143-102,591,285 MMP8
    nsv3330800copy number variation1nstd162human GRCh38 (hg38) chr11: 102,716,357-102,716,435 , GRCh37.p13 chr11: 102,587,088-102,587,166 MMP8
    nsv3330360insertion1nstd162human GRCh38 (hg38) chr11: 102,719,415-102,719,415 , GRCh37.p13 chr11: 102,590,146-102,590,146 MMP8
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