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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    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
    nsv7057432inversion1nstd229human GRCh38 chr4: 4,018,387-9,499,063 , GRCh37.p13 chr4: 4,020,114-9,500,707 CPZ, OR7E85P, 127 more genes
    nsv7056567inversion1nstd229human GRCh38 chr4: 8,352,143-8,456,003 , GRCh37.p13 chr4: 8,353,870-8,457,730 ACOX3, TRMT44, 1 more genes
    nsv7056110inversion1nstd229human GRCh38 chr4: 3,991,106-9,653,685 , GRCh37.p13 chr4: 3,992,833-9,655,309 MAN2B2, SH3TC1, 134 more genes
    nsv7055114inversion1nstd229human GRCh38 chr4: 8,400,925-10,237,375 , GRCh37.p13 chr4: 8,402,652-10,238,999 LOC101928948, SLC2A9-AS1, 65 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    nsv7041297inversion1nstd229human GRCh38 chr4: 8,440,641-8,464,828 , GRCh37.p13 chr4: 8,442,368-8,466,555 ACOX3, TRMT44
    nsv7039148inversion1nstd229human GRCh38 chr4: 4,150,240-8,956,846 , GRCh37.p13 chr4: 4,151,967-8,958,572 PPP2R2C, CRMP1, 80 more genes
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    nsv6737857copy number variation1nstd229human GRCh38 chr4: 8,460,549-8,532,772 , GRCh37.p13 chr4: 8,462,276-8,534,499 TRMT44
    nsv6736922copy number variation1nstd229human GRCh38 chr4: 8,439,080-8,504,722 , GRCh37.p13 chr4: 8,440,807-8,506,449 ACOX3, TRMT44
    nsv6733967copy number variation1nstd229human GRCh38 chr4: 8,438,095-8,456,285 , GRCh37.p13 chr4: 8,439,822-8,458,012 TRMT44, ACOX3
    nsv6733418copy number variation1nstd229human GRCh38 chr4: 8,304,727-8,567,777 , GRCh37.p13 chr4: 8,306,454-8,569,504 ACOX3, LINC02517, 3 more genes
    nsv6732879copy number variation1nstd229human GRCh38 chr4: 8,480,891-8,486,473 , GRCh37.p13 chr4: 8,482,618-8,488,200 TRMT44
    nsv6726867copy number variation1nstd229human GRCh38 chr4: 8,215,957-8,443,600 , GRCh37.p13 chr4: 8,217,684-8,445,327 ACOX3, SH3TC1, 5 more genes
    nsv6725776copy number variation1nstd229human GRCh38 chr4: 8,483,895-8,522,300 , GRCh37.p13 chr4: 8,485,622-8,524,027 TRMT44
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