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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979454inversion1nstd209human GRCh38 chr4: 68,478,582-68,481,837 , GRCh37.p13 chr4: 69,344,300-69,347,555 TMPRSS11E
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 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, 335 more genes
    nsv5346671translocation1nstd200human GRCh38 chr4: 68,456,340-68,456,340 , GRCh38 chr4: 68,456,267-68,456,267 , GRCh37.p13 chr4: 69,321,985-69,321,985 , GRCh37.p13 chr4: 69,322,058-69,322,058 TMPRSS11E
    nsv5176245mobile element insertion1nstd203human GRCh38 chr4: 68,473,775-68,473,791 , GRCh37.p13 chr4: 69,339,493-69,339,509 TMPRSS11E
    nsv5092238mobile element insertion1nstd203human GRCh38 chr4: 68,475,076-68,475,088 , GRCh37.p13 chr4: 69,340,794-69,340,806 TMPRSS11E
    nsv5090392mobile element insertion1nstd203human GRCh38 chr4: 68,494,191-68,494,207 , GRCh37.p13 chr4: 69,359,909-69,359,925 TMPRSS11E
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4922794copy number variation1nstd200human GRCh38 chr4: 68,447,710-68,448,652 , GRCh37.p13 chr4: 69,313,428-69,314,370 TMPRSS11E
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800080copy number variation1nstd200human GRCh37 chr4: 69,313,428-69,314,370 , GRCh38.p12 chr4: 68,447,710-68,448,652 TMPRSS11E
    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
    nsv4727993copy number variation4nstd197human GRCh37 chr4: 69,337,179-69,536,336 , GRCh38.p12 chr4: 68,471,461-68,670,618 UGT2B15, UGT2B17, 5 more genes
    nsv4674695copy number variation1nstd102humanUncertain significance GRCh37 chr4: 67,392,949-69,837,294 , GRCh38.p12 chr4: 66,527,231-68,971,576 ST3GAL1P1, UGT2B10, 47 more genes
    nsv4674399copy number variation1nstd102humanUncertain significance GRCh37 chr4: 66,948,561-69,631,390 , GRCh38.p12 chr4: 66,082,843-68,765,672 RNA5SP527, LOC100419046, 42 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
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