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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952013insertion1nstd209human GRCh38 chr6: 116,522,977-116,522,977 , GRCh37.p13 chr6: 116,844,140-116,844,140 CALHM5, TRAPPC3L
    nsv5689794mobile element insertion2nstd211human GRCh38 chr6: 116,522,993-116,522,993 , GRCh37.p13 chr6: 116,844,156-116,844,156 CALHM5, TRAPPC3L
    nsv5677136mobile element insertion2nstd211human GRCh38 chr6: 116,513,385-116,513,385 , GRCh37.p13 chr6: 116,834,548-116,834,548 CALHM5, TRAPPC3L
    nsv5628966insertion1nstd207human GRCh38 chr6: 116,522,977-116,522,977 , GRCh37.p13 chr6: 116,844,140-116,844,140 CALHM5, TRAPPC3L
    nsv5538445insertion1nstd206human GRCh38 chr6: 116,522,977-116,522,977 , GRCh37.p13 chr6: 116,844,140-116,844,140 TRAPPC3L, CALHM5
    nsv5468412copy number variation1nstd206human GRCh38 chr6: 116,512,367-116,520,366 , GRCh37.p13 chr6: 116,833,530-116,841,529 CALHM5, TRAPPC3L
    nsv5397478mobile element insertion1nstd206human GRCh38 chr6: 116,513,385-116,513,436 , GRCh37.p13 chr6: 116,834,548-116,834,599 CALHM5, TRAPPC3L
    nsv5369658translocation1nstd200human GRCh38 chr6: 116,514,077-116,514,077 , GRCh38 chr6: 116,514,144-116,514,144 , GRCh37.p13 chr6: 116,835,240-116,835,240 , GRCh37.p13 chr6: 116,835,307-116,835,307 CALHM5, TRAPPC3L
    nsv5340126translocation1nstd200human GRCh37 chr6: 116,835,240-116,835,240 , GRCh37 chr6: 116,835,307-116,835,307 , GRCh38.p12 chr6: 116,514,077-116,514,077 , GRCh38.p12 chr6: 116,514,144-116,514,144 CALHM5, TRAPPC3L
    nsv5115500mobile element insertion1nstd203human GRCh38 chr6: 116,522,993-116,522,997 , GRCh37.p13 chr6: 116,844,156-116,844,160 TRAPPC3L, CALHM5
    nsv5112371mobile element insertion1nstd203human GRCh38 chr6: 116,522,983-116,522,993 , GRCh37.p13 chr6: 116,844,146-116,844,156 TRAPPC3L, CALHM5
    nsv5111803mobile element insertion1nstd203human GRCh38 chr6: 116,522,984-116,522,993 , GRCh37.p13 chr6: 116,844,147-116,844,156 CALHM5, TRAPPC3L
    nsv5110297mobile element insertion1nstd203human GRCh38 chr6: 116,522,976-116,522,993 , GRCh37.p13 chr6: 116,844,139-116,844,156 CALHM5, TRAPPC3L
    nsv5107715mobile element insertion1nstd203human GRCh38 chr6: 116,522,981-116,522,993 , GRCh37.p13 chr6: 116,844,144-116,844,156 TRAPPC3L, CALHM5
    nsv5102966mobile element insertion1nstd203human GRCh38 chr6: 116,522,982-116,522,993 , GRCh37.p13 chr6: 116,844,145-116,844,156 CALHM5, TRAPPC3L
    nsv5100884mobile element insertion1nstd203human GRCh38 chr6: 116,545,366-116,545,384 , GRCh37.p13 chr6: 116,866,529-116,866,547 TRAPPC3L, CALHM4
    nsv5100410mobile element insertion1nstd203human GRCh38 chr6: 116,522,977-116,522,993 , GRCh37.p13 chr6: 116,844,140-116,844,156 TRAPPC3L, CALHM5
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4948353copy number variation1nstd200human GRCh38 chr6: 116,537,422-116,542,896 , GRCh37.p13 chr6: 116,858,585-116,864,059 TRAPPC3L, CALHM4
    nsv4768325copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959 GJA1, RNU4-76P, 80 more genes
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