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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911227copy number variation1nstd209human GRCh38 chr10: 43,401,088-43,401,167 , GRCh37.p13 chr10: 43,896,536-43,896,615 HNRNPF
    nsv5489204copy number variation1nstd206human GRCh38 chr10: 43,401,091-43,401,168 , GRCh37.p13 chr10: 43,896,539-43,896,616 HNRNPF
    nsv5481670copy number variation1nstd206human GRCh38 chr10: 43,391,155-43,392,367 , GRCh37.p13 chr10: 43,886,603-43,887,815 HNRNPF
    nsv5354387translocation1nstd200human GRCh38 chr10: 43,397,118-43,397,118 , GRCh38 chr10: 43,397,172-43,397,172 , GRCh37.p13 chr10: 43,892,620-43,892,620 , GRCh37.p13 chr10: 43,892,566-43,892,566 HNRNPF
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4969751copy number variation1nstd200human GRCh38 chr10: 43,401,318-43,401,599 , GRCh37.p13 chr10: 43,896,766-43,897,047 HNRNPF
    nsv4969750copy number variation1nstd200human GRCh38 chr10: 43,391,155-43,392,367 , GRCh37.p13 chr10: 43,886,603-43,887,815 HNRNPF
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4831927copy number variation1nstd200human GRCh37 chr10: 43,886,603-43,887,816 , GRCh38.p12 chr10: 43,391,155-43,392,368 HNRNPF
    nsv4614104copy number variation1nstd183human GRCh37 chr10: 43,891,693-43,932,595 , GRCh38.p12 chr10: 43,396,245-43,437,147 ZNF487, HNRNPF, 1 more genes
    nsv4609600copy number variation1nstd183human GRCh37 chr10: 43,881,063-43,881,851 , GRCh38.p12 chr10: 43,385,615-43,386,403 HNRNPF
    nsv4490466mobile element insertion1nstd166human GRCh37.p13 chr10: 43,894,458-43,894,458 , GRCh38.p12 chr10: 43,399,010-43,399,010 HNRNPF
    nsv4375959copy number variation1nstd173human GRCh37 chr10: 43,701,939-43,911,427 , GRCh38.p12 chr10: 43,206,491-43,415,979 HNRNPF, FXYD4, 7 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv4178309copy number variation1nstd166human GRCh37.p13 chr10: 43,900,077-43,901,871 , GRCh38.p12 chr10: 43,404,629-43,406,423 HNRNPF
    nsv4176596copy number variation1nstd166human GRCh37.p13 chr10: 43,896,766-43,897,047 , GRCh38.p12 chr10: 43,401,318-43,401,599 HNRNPF
    nsv4174797copy number variation1nstd166human GRCh37.p13 chr10: 43,896,539-43,896,616 , GRCh38.p12 chr10: 43,401,091-43,401,168 HNRNPF
    nsv4173462copy number variation1nstd166human GRCh37.p13 chr10: 43,891,002-43,891,505 , GRCh38.p12 chr10: 43,395,554-43,396,057 HNRNPF
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