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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5858426copy number variation1nstd209human GRCh38 chr9: 114,061,125-114,069,695 , GRCh37.p13 chr9: 116,823,405-116,831,975 AMBP
    nsv5852902copy number variation1nstd209human GRCh38 chr9: 114,052,898-114,062,574 , GRCh37.p13 chr9: 116,815,178-116,824,854 AMBP, ZNF618
    nsv5849140copy number variation1nstd209human GRCh38 chr9: 114,072,046-114,086,364 , GRCh37.p13 chr9: 116,834,326-116,848,644 LOC107987120, AMBP
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983285copy number variation1nstd200human GRCh38 chr9: 114,059,526-114,063,351 , GRCh37.p13 chr9: 116,821,806-116,825,631 AMBP
    nsv4836423copy number variation1nstd200human GRCh37 chr9: 116,821,806-116,825,631 , GRCh38.p12 chr9: 114,059,526-114,063,351 AMBP
    nsv4675840copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,642,144-117,613,527 , GRCh38.p12 chr9: 113,879,864-114,851,247 COL27A1, LOC107987120, 20 more genes
    nsv4675393copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,754,414-116,840,509 , GRCh38.p12 chr9: 113,992,134-114,078,229 AMBP, ZNF618, 1 more genes
    nsv4607614copy number variation1nstd183human GRCh37 chr9: 116,815,777-116,857,165 , GRCh38.p12 chr9: 114,053,497-114,094,885 LOC107987120, AMBP, 2 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
    nsv4456379copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,982,711-117,443,628 , GRCh38.p12 chr9: 111,220,431-114,681,348 MIR4668, LOC100418705, 74 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
    nsv4418570copy number variation1nstd174human GRCh37 chr9: 116,598,396-117,103,268 , GRCh38.p12 chr9: 113,836,116-114,340,988 ZNF618, MIR455, 11 more genes
    nsv4376157copy number variation1nstd173human GRCh37 chr9: 116,812,369-116,873,301 , GRCh38.p12 chr9: 114,050,089-114,111,021 LOC107987120, ZNF618, 2 more genes
    nsv4369087copy number variation1nstd173human GRCh37 chr9: 116,812,369-116,850,491 , GRCh38.p12 chr9: 114,050,089-114,088,211 AMBP, ZNF618, 1 more genes
    nsv4365976copy number variation1nstd173human GRCh37 chr9: 116,816,417-116,848,197 , GRCh38.p12 chr9: 114,054,137-114,085,917 AMBP, ZNF618, 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
    nsv4334096sequence alteration1nstd166human GRCh37.p13 chr9: 116,815,591-117,105,626 , GRCh38.p12 chr9: 114,053,311-114,343,346 ORM1, KIF12, 9 more genes
    nsv4176987copy number variation1nstd166human GRCh37.p13 chr9: 116,827,033-116,827,184 , GRCh38.p12 chr9: 114,064,753-114,064,904 AMBP
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
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