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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5274366copy number variation1nstd204human GRCh37.p13 chr11: 67,774,371-67,862,467 , GRCh38.p13 chr11: 68,006,901-68,095,000 ALDH3B1, CHKA, 5 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4715317copy number variation1nstd195human GRCh37 chr11: 67,743,201-68,242,601 , GRCh38.p12 chr11: 67,975,730-68,475,133 ALDH3B1, LRP5, 13 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 PPP1CA, RPS3AP40, 58 more genes
    nsv4617819copy number variation1nstd183human GRCh37 chr11: 67,810,635-67,810,985 , GRCh38.p12 chr11: 68,043,168-68,043,518 TCIRG1, MIR6753
    nsv4604827copy number variation1nstd183human GRCh37 chr11: 67,811,275-67,811,380 , GRCh38.p12 chr11: 68,043,808-68,043,913 TCIRG1, MIR6753
    nsv4414985copy number variation1nstd174human GRCh37 chr11: 67,747,160-67,821,610 , GRCh38.p12 chr11: 67,979,689-68,054,143 ALDH3B1, CHKA, 6 more genes
    nsv4367838copy number variation1nstd173human GRCh37 chr11: 67,410,235-67,812,234 , GRCh38.p12 chr11: 67,642,764-68,044,767 , OR7E11P, 24 more genes
    nsv3920906copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598 GRK2, ALDH3B1, 82 more genes
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    nsv3915534copy number variation1nstd102humanPathogenic NCBI36 chr11: 66,970,200-68,203,117 , GRCh38 chr11: 67,446,153-68,679,073 , GRCh37 chr11: 67,213,624-68,446,541 LOC107984343, PITPNM1, 46 more genes
    nsv3909768copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,799,160-70,701,268 , GRCh38.p12 chr11: 68,031,693-70,855,163 CCND1, CHKA, 56 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
    nsv3901678copy number variation1nstd102humanBenign GRCh37 chr11: 67,764,080-67,811,086 , GRCh38.p12 chr11: 67,996,609-68,043,619 MIR4691, NDUFS8, 5 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3167936inversion1nstd158human GRCh37 chr11: 64,590,560-68,196,411 , GRCh38.p12 chr11: 64,823,088-68,428,943 , ACTN3, 210 more genes
    nsv3149685copy number variation1nstd151human GRCh37 chr11: 67,799,616-67,816,469 , GRCh38.p12 chr11: 68,032,149-68,049,002 MIR4691, TCIRG1, 3 more genes
    nsv3147226copy number variation1nstd151human GRCh37 chr11: 67,786,637-67,864,602 , GRCh38.p12 chr11: 68,019,168-68,097,135 TCIRG1, MIR6753, 5 more genes
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