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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3886431copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,085-184,099,206 , GRCh38.p12 chr3: 184,379,297-184,381,418 CHRD, THPO
    nsv3889572copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,085-184,098,559 , GRCh38.p12 chr3: 184,379,297-184,380,771 CHRD, THPO
    nsv3882228copy number variation2nstd102humanBenign GRCh37 chr3: 184,097,736-184,099,206 , GRCh38.p12 chr3: 184,379,948-184,381,418 CHRD, THPO
    nsv3887153copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,736-184,098,559 , GRCh38.p12 chr3: 184,379,948-184,380,771 CHRD, THPO
    nsv3882175copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,736-184,098,466 , GRCh38.p12 chr3: 184,379,948-184,380,678 CHRD, THPO
    nsv3883368copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,847-184,098,559 , GRCh38.p12 chr3: 184,380,059-184,380,771 CHRD, THPO
    nsv3880908copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,787-184,098,466 , GRCh38.p12 chr3: 184,379,999-184,380,678 CHRD, THPO
    nsv3874459copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,847-184,098,517 , GRCh38.p12 chr3: 184,380,059-184,380,729 CHRD, THPO
    nsv3875258copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,787-184,098,193 , GRCh38.p12 chr3: 184,379,999-184,380,405 CHRD, THPO
    nsv3879834copy number variation1nstd102humanBenign GRCh37 chr3: 184,097,857-184,098,193 , GRCh38.p12 chr3: 184,380,069-184,380,405 CHRD, THPO
    nsv3914166copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506 CHRD, SNORA4, 199 more genes
    nsv3882335copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,650,681-191,275,809 , GRCh38.p12 chr3: 182,932,893-191,558,020 CHRD, VPS8, 171 more genes
    nsv6313539copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147 CHRD, ALG3, 133 more genes
    nsv6315366copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,556,940-188,083,060 , GRCh38.p12 chr3: 183,839,152-188,365,272 CHRD, MASP1, 115 more genes
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 CHRD, PRICKLE1P1, 99 more genes
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 CHRD, LOC105374253, 111 more genes
    nsv3886610copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,178,932-186,838,042 , GRCh38.p12 chr3: 183,461,144-187,120,254 CHRD, HTR3D, 104 more genes
    nsv4769252copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303 CHRD, LOC107986054, 83 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CHRD, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 CHRD, NDUFB4, 2876 more genes
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