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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 FDCSP, APOOP4, 147 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 338 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 MIR548AH, LOC105377271, 616 more genes
    nsv5089424mobile element insertion1nstd203human GRCh38 chr4: 70,659,013-70,659,028 , GRCh37.p13 chr4: 71,524,730-71,524,745 JCHAIN
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 LOC100129728, RPL22P13, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 MIR367, SMARCAD1, 913 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
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 LOC442113, LOC105377272, 248 more genes
    nsv4674737copy number variation1nstd102humanUncertain significance GRCh37 chr4: 71,193,683-71,591,539 , GRCh38.p12 chr4: 70,327,966-70,725,822 SMR3A, SMR3B, 12 more genes
    nsv4674141copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444 COX18, UGT2B11, 219 more genes
    nsv4476636mobile element insertion1nstd166human GRCh37.p13 chr4: 71,530,050-71,530,050 , GRCh38.p12 chr4: 70,664,333-70,664,333 JCHAIN
    nsv4476635mobile element insertion1nstd166human GRCh37.p13 chr4: 71,524,730-71,524,730 , GRCh38.p12 chr4: 70,659,013-70,659,013 JCHAIN
    nsv4456913copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,242,784-82,991,431 , GRCh38.p12 chr4: 67,377,066-82,070,278 CABS1, PPEF2, 273 more genes
    nsv4455423copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,929,700-72,479,262 , GRCh38.p12 chr4: 70,063,983-71,613,545 MOB1B, CSN3, 28 more genes
    nsv4099972copy number variation1nstd166human GRCh37.p13 chr4: 71,525,101-71,525,187 , GRCh38.p12 chr4: 70,659,384-70,659,470 JCHAIN
    nsv3924404copy number variation1nstd102humanUncertain significance NCBI36 chr4: 71,104,774-72,289,112 , GRCh37 chr4: 71,070,185-72,070,248 , GRCh38 chr4: 70,204,468-71,204,531 ODAM, CSN3, 20 more genes
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