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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5971322inversion1nstd209human GRCh38 chr5: 40,851,175-40,856,613 , GRCh37.p13 chr5: 40,851,277-40,856,715 CARD6
    nsv5969475inversion1nstd209human GRCh38 chr5: 40,846,083-40,848,655 , GRCh37.p13 chr5: 40,846,185-40,848,757 CARD6
    nsv5890211copy number variation1nstd209human GRCh38 chr5: 40,851,461-40,851,630 , GRCh37.p13 chr5: 40,851,563-40,851,732 CARD6
    nsv5842983copy number variation1nstd209human GRCh38 chr5: 40,848,333-40,851,182 , GRCh37.p13 chr5: 40,848,435-40,851,284 CARD6
    nsv5582169copy number variation1nstd207human GRCh38 chr5: 40,848,653-40,850,356 , GRCh37.p13 chr5: 40,848,755-40,850,458 CARD6
    nsv5568287copy number variation1nstd207human GRCh38 chr5: 40,850,428-40,851,073 , GRCh37.p13 chr5: 40,850,530-40,851,175 CARD6
    nsv5567437copy number variation1nstd207human GRCh38 chr5: 40,851,461-40,851,630 , GRCh37.p13 chr5: 40,851,563-40,851,732 CARD6
    nsv5559681sequence alteration1nstd206human GRCh38 chr5: 40,845,741-40,851,175 , GRCh37.p13 chr5: 40,845,843-40,851,277 CARD6
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5465841copy number variation1nstd206human GRCh38 chr5: 40,851,461-40,851,642 , GRCh37.p13 chr5: 40,851,563-40,851,744 CARD6
    nsv5462940copy number variation1nstd206human GRCh38 chr5: 40,836,060-40,840,202 , GRCh37.p13 chr5: 40,836,162-40,840,304 CARD6
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5368209translocation1nstd200human GRCh38 chr5: 40,851,176-40,851,176 , GRCh38 chr5: 40,845,742-40,845,742 , GRCh37.p13 chr5: 40,845,844-40,845,844 , GRCh37.p13 chr5: 40,851,278-40,851,278 CARD6
    nsv5344517translocation1nstd200human GRCh37 chr5: 40,848,758-40,848,758 , GRCh37 chr5: 40,846,188-40,846,188 , GRCh38.p12 chr5: 40,846,086-40,846,086 , GRCh38.p12 chr5: 40,848,656-40,848,656 CARD6
    nsv5336695translocation1nstd200human GRCh37 chr5: 40,845,844-40,845,844 , GRCh37 chr5: 40,851,278-40,851,278 , GRCh38.p12 chr5: 40,845,742-40,845,742 , GRCh38.p12 chr5: 40,851,176-40,851,176 CARD6
    nsv5321648translocation1nstd204human GRCh38.p13 chr5: 40,845,742-40,845,742 , GRCh38.p13 chr5: 40,851,176-40,851,176 , GRCh37.p13 chr5: 40,845,844-40,845,844 , GRCh37.p13 chr5: 40,851,278-40,851,278 CARD6
    nsv5228904copy number variation1nstd204human GRCh38.p13 chr5: 40,848,333-40,851,632 , GRCh37.p13 chr5: 40,848,435-40,851,734 CARD6
    nsv5228601copy number variation1nstd204human GRCh38.p13 chr5: 40,848,701-40,850,800 , GRCh37.p13 chr5: 40,848,803-40,850,902 CARD6
    nsv5095901mobile element insertion1nstd203human GRCh38 chr5: 40,847,759-40,847,773 , GRCh37.p13 chr5: 40,847,861-40,847,875 CARD6
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