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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960887insertion1nstd209human GRCh38 chr6: 170,568,765-170,568,765 , GRCh37.p13 chr6: 170,877,853-170,877,853 TBP
    nsv5845153copy number variation1nstd209human GRCh38 chr6: 170,552,636-170,555,212 , GRCh37.p13 chr6: 170,861,724-170,864,300 PSMB1, TBP
    nsv5454360copy number variation1nstd206human GRCh38 chr6: 170,559,000-170,615,393 , GRCh37.p13 chr6: 170,868,088-170,924,481 TBP, PDCD2
    nsv5100787mobile element insertion1nstd203human GRCh38 chr6: 170,552,340-170,552,354 , GRCh37.p13 chr6: 170,861,428-170,861,442 TBP, PSMB1
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4729261copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,580,012-170,919,482 , GRCh38.p12 chr6: 167,166,524-170,610,394 LOC107986549, AFDN, 81 more genes
    nsv4675958copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,440,417-170,919,482 , GRCh38.p12 chr6: 167,026,929-170,610,394 CCR6, HGC6.3, 86 more genes
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
    nsv4675577copy number variation1nstd102humanPathogenic GRCh37 chr6: 170,136,337-170,919,482 , GRCh38.p12 chr6: 169,736,241-170,610,394 LOC107986676, LOC105378149, 22 more genes
    nsv4675360copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 170,331,096-170,919,482 , GRCh38.p12 chr6: 170,015,872-170,610,394 PDCD2, PSMB1, 14 more genes
    nsv4675281copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394 LOC105378127, LOC105378130, 148 more genes
    nsv4605951copy number variation1nstd183human GRCh37 chr6: 170,864,731-170,900,391 , GRCh38.p12 chr6: 170,555,643-170,591,303 TBP, PDCD2
    nsv4457317copy number variation1nstd102humanUncertain significance GRCh37 chr6: 170,653,923-170,919,482 , GRCh38.p12 chr6: 170,344,835-170,610,394 , GRCh38.p12 chr6|NT_187553.1: 72,073-271,782 LOC107986676, TBP, 4 more genes
    nsv4457190copy number variation1nstd102humanUncertain significance GRCh37 chr6: 170,799,449-170,864,758 , GRCh38.p12 chr6: 170,490,361-170,555,670 , GRCh38.p12 chr6|NT_187553.1: 226,922-271,782 PSMB1, LOC105378157, 1 more genes
    nsv4455397copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,607,593-170,919,482 , GRCh38.p12 chr6: 166,194,105-170,610,394 TBP, LOC112267970, 108 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4403518copy number variation1nstd174human GRCh37 chr6: 170,864,719-170,910,378 , GRCh38.p12 chr6: 170,555,631-170,601,290 PDCD2, TBP
    nsv4379598copy number variation1nstd173human GRCh37 chr6: 170,822,161-170,879,054 , GRCh38.p12 chr6: 170,513,073-170,569,966 PSMB1, TBP
    nsv4378089copy number variation2nstd173human GRCh37 chr6: 170,875,684-170,919,482 , GRCh38.p12 chr6: 170,566,596-170,610,394 , TBP, 1 more genes
    nsv4376081copy number variation1nstd173human GRCh37 chr6: 163,617,482-170,919,482 , GRCh38.p12 chr6: 163,196,450-170,610,394 , LOC107986550, 151 more genes
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