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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122256copy number variation1nstd186human GRCh37 chr16: 18,530,808-18,703,808 , GRCh38.p12 chr16: 18,519,486-18,692,486 NOMO2, ABCC6P1
    nsv6122171copy number variation1nstd186human GRCh37 chr16: 18,569,936-18,645,886 , GRCh38.p12 chr16: 18,558,614-18,634,564 NOMO2, ABCC6P1
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv5969472inversion1nstd209human GRCh38 chr16: 16,657,579-18,701,513 , GRCh37.p13 chr16: 16,751,436-18,712,835 , XYLT1, 28 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5882723copy number variation2nstd209human GRCh38 chr16: 18,570,672-18,589,639 , GRCh37.p13 chr16: 18,581,994-18,600,961 ABCC6P1
    nsv5868433copy number variation2nstd209human GRCh38 chr16: 18,595,297-18,602,242 , GRCh37.p13 chr16: 18,606,619-18,613,564 ABCC6P1
    nsv5527343copy number variation1nstd206human GRCh38 chr16: 18,596,321-18,599,201 , GRCh37.p13 chr16: 18,607,643-18,610,523 ABCC6P1
    nsv5526945copy number variation1nstd206human GRCh38 chr16: 18,558,614-18,634,564 , GRCh37.p13 chr16: 18,569,936-18,645,886 NOMO2, ABCC6P1
    nsv5520820copy number variation1nstd206human GRCh38 chr16: 18,490,486-18,600,486 , GRCh37.p13 chr16: 18,530,344-18,611,808 LOC105379460, MIR3179-4, 2 more genes
    nsv5520558copy number variation1nstd206human GRCh38 chr16: 18,519,486-18,692,486 , GRCh37.p13 chr16: 18,530,808-18,703,808 ABCC6P1, NOMO2
    nsv5380983copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,968,859-16,363,239 , GRCh38.p12 chr16: 14,875,002-16,269,382 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,927,385 LOC102724984, LOC728138, 50 more genes
    nsv5279746copy number variation1nstd204human GRCh38.p13 chr16: 18,595,322-18,601,554 , GRCh37.p13 chr16: 18,606,644-18,612,876 ABCC6P1
    nsv5279506copy number variation1nstd204human GRCh38.p13 chr16: 18,579,910-18,583,583 , GRCh37.p13 chr16: 18,591,232-18,594,905 ABCC6P1
    nsv5278948copy number variation1nstd204human GRCh38.p13 chr16: 18,583,384-18,585,431 , GRCh37.p13 chr16: 18,594,706-18,596,753 ABCC6P1
    nsv5278644copy number variation1nstd204human GRCh38.p13 chr16: 18,575,307-18,578,813 , GRCh37.p13 chr16: 18,586,629-18,590,135 ABCC6P1
    nsv5276997copy number variation1nstd204human GRCh38.p13 chr16: 18,586,583-18,589,012 , GRCh37.p13 chr16: 18,597,905-18,600,334 ABCC6P1
    nsv5271989copy number variation1nstd204human GRCh38.p13 chr16: 18,595,001-18,669,600 , GRCh37.p13 chr16: 18,606,323-18,680,922 ABCC6P1
    nsv5269883copy number variation1nstd204human GRCh38.p13 chr16: 18,570,829-18,573,242 , GRCh37.p13 chr16: 18,582,151-18,584,564 ABCC6P1
    nsv5269541copy number variation1nstd204human GRCh38.p13 chr16: 18,557,851-18,587,595 , GRCh37.p13 chr16: 18,569,173-18,598,917 NOMO2, ABCC6P1
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