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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7055708inversion1nstd229human GRCh38 chr4: 2,492,114-2,505,477 , GRCh37.p13 chr4: 2,493,841-2,507,204 RNF4
    nsv7049289inversion1nstd229human GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139 RNF4, SCARNA22, 28 more genes
    nsv7039441inversion1nstd229human GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175 NOP14-AS1, LOC112268460, 34 more genes
    nsv6735891copy number variation1nstd229human GRCh38 chr4: 2,483,108-2,489,213 , GRCh37.p13 chr4: 2,484,835-2,490,940 RNF4
    nsv6735530copy number variation1nstd229human GRCh38 chr4: 2,445,793-2,508,353 , GRCh37.p13 chr4: 2,447,520-2,510,080 LOC105374353, CFAP99, 2 more genes
    nsv6732036copy number variation1nstd229human GRCh38 chr4: 2,460,623-2,474,121 , GRCh37.p13 chr4: 2,462,350-2,475,848 LOC107986250, RNF4, 2 more genes
    nsv6730394copy number variation1nstd229human GRCh38 chr4: 2,200,486-2,609,402 , GRCh37.p13 chr4: 2,202,213-2,611,129 MIR4800, LOC105374352, 13 more genes
    nsv6728757copy number variation1nstd229human GRCh38 chr4: 2,470,574-2,473,419 , GRCh37.p13 chr4: 2,472,301-2,475,146 RNF4
    nsv6725535copy number variation1nstd229human GRCh38 chr4: 2,201,001-2,480,600 , GRCh37.p13 chr4: 2,202,728-2,482,327 POLN, RNF4, 12 more genes
    nsv6725051copy number variation1nstd229human GRCh38 chr4: 2,246,401-2,512,800 , GRCh37.p13 chr4: 2,248,128-2,514,527 LOC105374353, ZFYVE28, 9 more genes
    nsv6723468copy number variation1nstd229human GRCh38 chr4: 2,472,546-2,474,289 , GRCh37.p13 chr4: 2,474,273-2,476,016 RNF4
    nsv6722387copy number variation1nstd229human GRCh38 chr4: 2,471,468-2,471,504 , GRCh37.p13 chr4: 2,473,195-2,473,231 RNF4
    nsv6637013copy number variation1nstd102humanUncertain significance GRCh37 chr4: 2,195,665-2,503,033 , GRCh38.p12 chr4: 2,193,938-2,501,306 LOC105374352, POLN, 12 more genes
    nsv6636600copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,892,740-2,503,033 , GRCh38.p12 chr4: 1,891,013-2,501,306 LOC105374352, POLN, 19 more genes
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636534copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 963,688-2,913,553 , GRCh38.p12 chr4: 969,900-2,911,826 ADD1, CTBP1, 53 more genes
    nsv6636256copy number variation1nstd102humanPathogenic GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377 AFAP1-AS1, LOC389199, 294 more genes
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