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Items: 1 to 20 of 191103

  • The following terms were not found in dbVar: Levofloxacin, impurity.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877772copy number variation1nstd102humanPathogenic GRCh38 chr8: 86,667,104-86,675,513 , GRCh37 chr8: 87,679,332-87,687,741 CNGB3
    nsv4452567copy number variation1nstd102humanPathogenic GRCh38 chr8: 100,182,304-100,184,656 , GRCh37 chr8: 101,194,532-101,196,884 SPAG1
    nsv7098983copy number variation1nstd102humanPathogenic GRCh38 chr8: 30,679,021-30,681,266 , GRCh37 chr8: 30,536,538-30,538,783 GSR
    nsv7093052copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,638,780-145,639,772 , GRCh38 chr8: 144,413,396-144,414,388 SLC39A4
    nsv6634633copy number variation1nstd102humanPathogenic GRCh37 chr8: 117,860,986-117,861,652 , GRCh38 chr8: 116,848,747-116,849,413 RAD21
    nsv4454499copy number variation1nstd102humanPathogenic GRCh37 chr8: 101,199,328-101,199,498 , GRCh38 chr8: 100,187,100-100,187,270 SPAG1
    nsv997137copy number variation1nstd45humanPathogenic GRCh38.p12 chr8: 115,408,496-115,669,028 , GRCh37 chr8: 116,420,724-116,681,255 TRPS1
    nsv997108copy number variation1nstd45humanPathogenic GRCh38.p12 chr8: 60,678,765-60,868,028 , GRCh37 chr8: 61,591,324-61,780,587 CHD7
    nsv6137858copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,813,474-19,815,538 , GRCh38.p12 chr8: 19,955,963-19,958,027 LPL
    nsv6314350complex chromosomal rearrangement2nstd102humanPathogenic GRCh38.p12 chr9: 21,845,449-21,845,449 , GRCh38.p12 chr9: 21,845,457-21,845,457 , GRCh37 chr9: 21,845,448-21,845,448 , GRCh37 chr9: 21,845,456-21,845,456 , GRCh38.p12 chr8: 59,982,704-59,982,704 , GRCh38.p12 chr8: 59,982,708-59,982,708 , GRCh37 chr8: 60,895,263-60,895,263 , GRCh37 chr8: 60,895,267-60,895,267 MTAP
    nsv3884481copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 3,914,469-4,157,437 , GRCh37.p13 chr8: 3,771,991-4,014,959 CSMD1
    nsv3873273copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 3,876,145-3,961,401 , GRCh37.p13 chr8: 3,733,667-3,818,923 CSMD1
    nsv3870937copy number variation1nstd102humanLikely pathogenic GRCh38 chr8: 4,410,048-4,458,635 , GRCh37.p13 chr8: 4,267,570-4,316,157 CSMD1
    nsv6314404complex chromosomal rearrangement2nstd102humanLikely pathogenic GRCh38.p12 chr8: 18,716,567-18,716,567 , GRCh38.p12 chr8: 18,716,568-18,716,568 , GRCh37 chr8: 18,574,077-18,574,077 , GRCh37 chr8: 18,574,078-18,574,078 , GRCh38.p12 chr2: 199,227,700-199,227,700 , GRCh38.p12 chr2: 199,227,701-199,227,701 , GRCh37 chr2: 200,092,423-200,092,423 , GRCh37 chr2: 200,092,424-200,092,424 PSD3
    nsv3890129copy number variation1nstd102humanLikely benign GRCh37 chr8: 10,447,116-10,504,819 , GRCh38.p12 chr8: 10,589,606-10,647,309 , GRCh38.p12 chr8|NW_018654717.1: 2,699,773-2,757,432 RP1L1
    nsv3890721copy number variation1nstd102humanLikely benign GRCh37 chr8: 71,608,781-71,646,728 , GRCh38.p12 chr8: 70,696,546-70,734,493 XKR9
    nsv3890719copy number variation1nstd102humanBenign GRCh37 chr8: 4,323,965-4,359,306 , GRCh38.p12 chr8: 4,466,443-4,501,784 CSMD1
    nsv3908216copy number variation1nstd102humanBenign GRCh37 chr8: 3,619,348-3,650,542 , GRCh38.p12 chr8: 3,761,826-3,793,020 CSMD1
    nsv3887819copy number variation1nstd102humanUncertain significance NCBI36 chr8: 3,841,790-4,124,804 , GRCh37.p13 chr8: 3,854,382-4,137,396 , GRCh38.p12 chr8: 3,996,860-4,279,874 CSMD1
    nsv3905167copy number variation1nstd102humanUncertain significance GRCh37 chr8: 109,990,022-110,168,343 , GRCh38.p12 chr8: 108,977,793-109,156,114 TRHR
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