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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5471699copy number variation1nstd206human GRCh38 chr4: 184,787,735-184,847,892 , GRCh37.p13 chr4: 185,708,889-185,769,046 MIR3945HG, ACSL1, 2 more genes
    nsv5454803copy number variation1nstd206human GRCh38 chr4: 184,212,885-185,009,149 , GRCh37.p13 chr4: 185,134,038-185,930,303 , RPL6P16, 22 more genes
    nsv5227634copy number variation1nstd204human GRCh38.p13 chr4: 184,783,922-184,816,404 , GRCh37.p13 chr4: 185,705,076-185,737,558 SLED1, ACSL1
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    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
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4674658copy number variation1nstd102humanPathogenic GRCh37 chr4: 178,566,256-190,957,473 , GRCh38.p12 chr4: 177,645,102-190,036,318 RARRES2P4, ING2-DT, 165 more genes
    nsv4674432copy number variation1nstd102humanUncertain significance GRCh37 chr4: 184,695,117-185,817,439 , GRCh38.p12 chr4: 183,773,964-184,896,285 SLED1, LINC02365, 22 more genes
    nsv4674146copy number variation1nstd102humanPathogenic GRCh37 chr4: 179,752,903-187,987,047 , GRCh38.p12 chr4: 178,831,749-187,065,893 LINC02365, LINC02437, 105 more genes
    nsv4674043copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318 CYP4V2, ZFP42, 319 more genes
    nsv4673933copy number variation1nstd102humanUncertain significance GRCh37 chr4: 185,211,828-185,748,806 , GRCh38.p12 chr4: 184,290,675-184,827,652 CASP3, CENPU, 12 more genes
    nsv4578581copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 183,245,174-190,948,359 , GRCh38.p12 chr4: 182,324,021-190,027,204 SLC25A4, CASP3, 140 more genes
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4457076copy number variation1nstd102humanUncertain significance GRCh37 chr4: 185,399,884-186,542,127 , GRCh38.p12 chr4: 184,478,730-185,620,973 LINC02436, CENPU, 27 more genes
    nsv4456954copy number variation1nstd102humanPathogenic GRCh37 chr4: 184,648,532-190,957,473 , GRCh38.p12 chr4: 183,727,379-190,036,318 LINC02365, LINC02434, 110 more genes
    nsv4456349copy number variation1nstd102humanPathogenic GRCh37 chr4: 179,996,712-190,957,473 , GRCh38.p12 chr4: 179,075,558-190,036,318 MRPS36P2, RNA5SP174, 155 more genes
    nsv4456171copy number variation1nstd102humanPathogenic GRCh37 chr4: 166,623,890-190,957,473 , GRCh38.p12 chr4: 165,702,738-190,036,318 TRIML2, LTO1P1, 284 more genes
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