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Items: 1 to 20 of 173

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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 , DCK, 147 more genes
    nsv5685363mobile element insertion1nstd211human GRCh38 chr4: 70,640,032-70,640,032 , GRCh37.p13 chr4: 71,505,749-71,505,749 ENAM
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5402793mobile element insertion1nstd206human GRCh38 chr4: 70,640,032-70,640,083 , GRCh37.p13 chr4: 71,505,749-71,505,800 ENAM
    nsv5239235copy number variation1nstd204human GRCh38.p13 chr4: 70,602,716-70,640,707 , GRCh37.p13 chr4: 71,468,433-71,506,424 ENAM, AMBN
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 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 PTPN11P5, LOC643014, 244 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, 216 more genes
    nsv4597443copy number variation1nstd183human GRCh37 chr4: 71,462,680-71,507,755 , GRCh38.p12 chr4: 70,596,963-70,642,038 ENAM, AMBN
    nsv4591468copy number variation1nstd183human GRCh37 chr4: 71,511,744-71,512,554 , GRCh38.p12 chr4: 70,646,027-70,646,837 ENAM
    nsv4475921mobile element insertion1nstd166human GRCh37.p13 chr4: 71,493,695-71,493,695 , GRCh38.p12 chr4: 70,627,978-70,627,978 ENAM
    nsv4456913copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,242,784-82,991,431 , GRCh38.p12 chr4: 67,377,066-82,070,278 KPNA2P1, CCNG2, 270 more genes
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