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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5893600copy number variation1nstd209human GRCh38 chr4: 3,444,165-3,448,342 , GRCh37.p13 chr4: 3,445,892-3,450,069 , HGFAC
    nsv5673743copy number variation1nstd102humanPathogenic GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513 ZFYVE28, LINC01587, 81 more genes
    nsv5623450insertion1nstd207human GRCh38 chr4: 3,440,813-3,440,813 , GRCh37.p13 chr4: 3,442,540-3,442,540 HGFAC
    nsv5613574insertion1nstd207human GRCh38 chr4: 3,440,674-3,440,674 , GRCh37.p13 chr4: 3,442,401-3,442,401 HGFAC
    nsv5582986copy number variation1nstd207human GRCh38 chr4: 3,440,721-3,440,773 , GRCh37.p13 chr4: 3,442,448-3,442,500 HGFAC
    nsv5565118copy number variation1nstd207human GRCh38 chr4: 3,440,632-3,440,773 , GRCh37.p13 chr4: 3,442,359-3,442,500 HGFAC
    nsv5440006copy number variation1nstd206human GRCh38 chr4: 3,444,119-3,448,343 , GRCh37.p13 chr4: 3,445,846-3,450,070 , HGFAC
    nsv5439883copy number variation1nstd206human GRCh38 chr4: 3,442,792-3,443,209 , GRCh37.p13 chr4: 3,444,519-3,444,936 HGFAC
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
    nsv5341530translocation1nstd200human GRCh37 chr4: 3,445,895-3,445,895 , GRCh37 chr4: 3,450,070-3,450,070 , GRCh38.p12 chr4: 3,444,168-3,444,168 , GRCh38.p12 chr4: 3,448,343-3,448,343 , HGFAC
    nsv5319088copy number variation1nstd204human GRCh37.p13 chr4: 3,445,894-3,450,071 , GRCh38.p13 chr4: 3,444,167-3,448,344 , HGFAC
    nsv5233880copy number variation1nstd204human GRCh38.p13 chr4: 3,444,115-3,448,614 , GRCh37.p13 chr4: 3,445,842-3,450,341 , HGFAC
    nsv4912927copy number variation1nstd200human GRCh38 chr4: 3,444,168-3,448,343 , GRCh37.p13 chr4: 3,445,895-3,450,070 , HGFAC
    nsv4799192copy number variation1nstd200human GRCh37 chr4: 3,444,519-3,444,936 , GRCh38.p12 chr4: 3,442,792-3,443,209 HGFAC
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
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