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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
    nsv5673649copy number variation1nstd102humanPathogenic GRCh37 chr4: 1,619,775-2,181,192 , GRCh38.p12 chr4: 1,618,048-2,179,465 NSD2, TMEM129, 15 more genes
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
    nsv5321288translocation1nstd204human GRCh38.p13 chr4: 2,059,409-2,059,409 , GRCh38.p13 chr4: 2,059,484-2,059,484 , GRCh37.p13 chr4: 2,061,136-2,061,136 , GRCh37.p13 chr4: 2,061,211-2,061,211 NAT8L
    nsv5312240copy number variation1nstd204human GRCh38.p13 chr4: 2,059,101-2,059,498 , GRCh37.p13 chr4: 2,060,828-2,061,225 NAT8L
    nsv5238617copy number variation1nstd204human GRCh38.p13 chr4: 2,068,701-2,075,600 , GRCh37.p13 chr4: 2,070,428-2,077,327 NAT8L, POLN
    nsv5226239copy number variation1nstd204human GRCh38.p13 chr4: 2,057,553-2,060,350 , GRCh37.p13 chr4: 2,059,280-2,062,077 NAT8L
    nsv4912860copy number variation1nstd200human GRCh38 chr4: 2,068,180-2,068,318 , GRCh37.p13 chr4: 2,069,907-2,070,045 NAT8L
    nsv4912859copy number variation1nstd200human GRCh38 chr4: 2,054,859-2,057,337 , GRCh37.p13 chr4: 2,056,586-2,059,064 NAT8L
    nsv4799135copy number variation1nstd200human GRCh37 chr4: 2,056,588-2,059,064 , GRCh38.p12 chr4: 2,054,861-2,057,337 NAT8L
    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
    nsv4729500copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-2,503,033 , GRCh38.p12 chr4: 68,453-2,501,306 MIR4800, NELFA, 80 more genes
    nsv4729483copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-2,137,211 , GRCh38.p12 chr4: 68,453-2,135,484 LOC105374348, ZNF721, 67 more genes
    nsv4729295copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-5,831,521 , GRCh38.p12 chr4: 68,453-5,829,794 FGFR3, NICOL1, 151 more genes
    nsv4729016copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-5,046,326 , GRCh38.p12 chr4: 68,453-5,044,599 TMEM175, LOC105374346, 145 more genes
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