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Items: 1 to 20 of 406

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112732copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,200-4,012,072 , GRCh38.p12 chr5: 13,200-4,011,958 SLC9A3-AS1, LOC107984098, 76 more genes
    nsv5968719inversion1nstd209human GRCh38 chr5: 239,340-1,590,367 , GRCh37.p13 chr5: 239,455-1,590,482 , SDHA, 43 more genes
    nsv5906288copy number variation1nstd209human GRCh38 chr5: 897,258-899,882 , GRCh37.p13 chr5: 897,373-899,997 TRIP13
    nsv5900640copy number variation1nstd209human GRCh38 chr5: 734,052-922,928 , GRCh37.p13 chr5: 734,167-923,043 , TRIP13, 4 more genes
    nsv5843817copy number variation2nstd209human GRCh38 chr5: 902,013-903,212 , GRCh37.p13 chr5: 902,128-903,327 TRIP13
    nsv5843579copy number variation2nstd209human GRCh38 chr5: 919,584-920,983 , GRCh37.p13 chr5: 919,699-921,098 TRIP13
    nsv5843577copy number variation2nstd209human GRCh38 chr5: 904,828-905,827 , GRCh37.p13 chr5: 904,943-905,942 TRIP13
    nsv5685442mobile element insertion2nstd211human GRCh38 chr5: 917,537-917,537 , GRCh37.p13 chr5: 917,652-917,652 TRIP13
    nsv5640777insertion1nstd207human GRCh38 chr5: 899,655-899,655 , GRCh37.p13 chr5: 899,770-899,770 TRIP13
    nsv5638428insertion1nstd207human GRCh38 chr5: 897,348-897,348 , GRCh37.p13 chr5: 897,463-897,463 TRIP13
    nsv5584067copy number variation1nstd207human GRCh38 chr5: 898,505-898,965 , GRCh37.p13 chr5: 898,620-899,080 TRIP13
    nsv5582934copy number variation1nstd207human GRCh38 chr5: 897,411-897,872 , GRCh37.p13 chr5: 897,526-897,987 TRIP13
    nsv5581194copy number variation1nstd207human GRCh38 chr5: 898,005-898,466 , GRCh37.p13 chr5: 898,120-898,581 TRIP13
    nsv5580651copy number variation1nstd207human GRCh38 chr5: 915,397-915,452 , GRCh37.p13 chr5: 915,512-915,567 TRIP13
    nsv5572691copy number variation1nstd207human GRCh38 chr5: 897,282-899,851 , GRCh37.p13 chr5: 897,397-899,966 TRIP13
    nsv5567285copy number variation1nstd207human GRCh38 chr5: 898,797-898,994 , GRCh37.p13 chr5: 898,912-899,109 TRIP13
    nsv5567164copy number variation1nstd207human GRCh38 chr5: 897,348-898,337 , GRCh37.p13 chr5: 897,463-898,452 TRIP13
    nsv5465529copy number variation1nstd206human GRCh38 chr5: 897,248-899,946 , GRCh37.p13 chr5: 897,363-900,061 TRIP13
    nsv5401334mobile element insertion1nstd206human GRCh38 chr5: 917,537-917,588 , GRCh37.p13 chr5: 917,652-917,703 TRIP13
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
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