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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    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
    nsv4944120copy number variation1nstd200human GRCh38 chr4: 183,509,739-183,794,572 , GRCh37.p13 chr4: 184,430,892-184,715,725 , LOC105377581, 10 more genes
    nsv4802046copy number variation1nstd200human GRCh37 chr4: 184,425,977-184,426,323 , GRCh38.p12 chr4: 183,504,824-183,505,170 ING2-DT, ING2
    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
    nsv4729375copy number variation1nstd102humanPathogenic GRCh37 chr4: 169,108,358-184,425,536 , GRCh38.p12 chr4: 168,187,207-183,504,383 GALNT7-DT, LOC105377524, 154 more genes
    nsv4728923copy number variation1nstd102humanUncertain significance GRCh37 chr4: 181,853,722-184,723,116 , GRCh38.p12 chr4: 180,932,569-183,801,963 RNU6-479P, LOC105377581, 41 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
    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
    nsv4590540copy number variation1nstd183human GRCh37 chr4: 184,418,821-184,427,600 , GRCh38.p12 chr4: 183,497,668-183,506,447 ING2, ING2-DT
    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
    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
    nsv4456121copy number variation2nstd102humanUncertain significance GRCh37 chr4: 183,712,263-185,501,647 , GRCh38.p12 chr4: 182,791,110-184,580,493 CDKN2AIP, LOC105377584, 41 more genes
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