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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911439copy number variation1nstd209human GRCh38 chr9: 97,690,517-97,690,649 , GRCh37.p13 chr9: 100,452,799-100,452,931 XPA
    nsv5561999mobile element insertion1nstd206human GRCh38 chr9: 97,692,708-97,692,708 , GRCh37.p13 chr9: 100,454,990-100,454,990 XPA
    nsv5483600copy number variation1nstd206human GRCh38 chr9: 97,690,533-97,690,633 , GRCh37.p13 chr9: 100,452,815-100,452,915 XPA
    nsv5476170copy number variation1nstd206human GRCh38 chr9: 97,596,188-97,658,373 , GRCh37.p13 chr9: 100,358,470-100,420,655 , TMOD1, 3 more genes
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv4982696copy number variation1nstd200human GRCh38 chr9: 97,690,596-97,714,962 , GRCh37.p13 chr9: 100,452,878-100,477,244 KRT18P13, XPA, 1 more genes
    nsv4982695copy number variation1nstd200human GRCh38 chr9: 97,690,533-97,690,633 , GRCh37.p13 chr9: 100,452,815-100,452,915 XPA
    nsv4824178copy number variation1nstd200human GRCh37 chr9: 100,452,878-100,477,244 , GRCh38.p12 chr9: 97,690,596-97,714,962 XPA, PTCSC2, 1 more genes
    nsv4824177copy number variation1nstd200human GRCh37 chr9: 100,446,196-100,446,409 , GRCh38.p12 chr9: 97,683,914-97,684,127 XPA
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4683944copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,190,728-101,558,793 , GRCh38.p12 chr9: 97,428,446-98,796,511 TRMO, RNU6-918P, 20 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4675319copy number variation1nstd102humanLikely benign GRCh37 chr9: 100,306,203-100,528,811 , GRCh38.p12 chr9: 97,543,921-97,766,529 KRT18P13, PTCSC2, 4 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456610copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,310,710-100,535,203 , GRCh38.p12 chr9: 97,548,428-97,772,921 PTCSC2, TMOD1, 4 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4384504copy number variation1nstd173human GRCh37 chr9: 100,446,391-100,474,286 , GRCh38.p12 chr9: 97,684,109-97,712,004 XPA, KRT18P13, 1 more genes
    nsv4371381copy number variation1nstd173human GRCh37 chr9: 100,446,391-100,474,285 , GRCh38.p12 chr9: 97,684,109-97,712,003 XPA, PTCSC2, 1 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4184111copy number variation1nstd166human GRCh37.p13 chr9: 100,452,815-100,452,915 , GRCh38.p12 chr9: 97,690,533-97,690,633 XPA
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