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Items: 1 to 20 of 353

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978852insertion1nstd209human GRCh38 chr11: 17,874,884-17,874,884 , GRCh37.p13 chr11: 17,896,431-17,896,431 SERGEF
    nsv5978552insertion1nstd209human GRCh38 chr11: 17,925,267-17,925,267 , GRCh37.p13 chr11: 17,946,814-17,946,814 SERGEF
    nsv5976231insertion1nstd209human GRCh38 chr11: 17,836,382-17,836,382 , GRCh37.p13 chr11: 17,857,929-17,857,929 SERGEF
    nsv5922327copy number variation1nstd209human GRCh38 chr11: 17,925,267-17,925,345 , GRCh37.p13 chr11: 17,946,814-17,946,892 SERGEF
    nsv5850172copy number variation1nstd209human GRCh38 chr11: 17,815,240-17,824,172 , GRCh37.p13 chr11: 17,836,787-17,845,719 SERGEF
    nsv5708126mobile element insertion2nstd211human GRCh38 chr11: 17,878,988-17,878,988 , GRCh37.p13 chr11: 17,900,535-17,900,535 SERGEF
    nsv5585664copy number variation1nstd207human GRCh38 chr11: 17,925,188-17,925,266 , GRCh37.p13 chr11: 17,946,735-17,946,813 SERGEF
    nsv5536827insertion1nstd206human GRCh38 chr11: 17,874,884-17,874,887 , GRCh37.p13 chr11: 17,896,431-17,896,434 SERGEF
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5506874copy number variation1nstd206human GRCh38 chr11: 17,877,275-17,878,524 , GRCh37.p13 chr11: 17,898,822-17,900,071 SERGEF
    nsv5497175copy number variation1nstd206human GRCh38 chr11: 17,999,507-18,006,943 , GRCh37.p13 chr11: 18,021,054-18,028,490 SERGEF
    nsv5405310mobile element insertion1nstd206human GRCh38 chr11: 17,878,988-17,879,039 , GRCh37.p13 chr11: 17,900,535-17,900,586 SERGEF
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv5354785translocation1nstd200human GRCh38 chr11: 18,000,264-18,000,264 , GRCh38 chr11: 18,002,789-18,002,789 , GRCh37.p13 chr11: 18,021,811-18,021,811 , GRCh37.p13 chr11: 18,024,336-18,024,336 SERGEF
    nsv5341183translocation1nstd200human GRCh37 chr11: 17,984,956-17,984,956 , GRCh37 chr11: 17,984,876-17,984,876 , GRCh38.p12 chr11: 17,963,329-17,963,329 , GRCh38.p12 chr11: 17,963,409-17,963,409 SERGEF
    nsv5325213translocation1nstd204human GRCh38.p13 chr11: 17,812,993-17,812,993 , GRCh38.p13 chr11: 17,815,057-17,815,057 , GRCh37.p13 chr11: 17,834,540-17,834,540 , GRCh37.p13 chr11: 17,836,604-17,836,604 SERGEF
    nsv5260359copy number variation1nstd204human GRCh38.p13 chr11: 17,813,001-17,815,000 , GRCh37.p13 chr11: 17,834,548-17,836,547 SERGEF
    nsv5193652mobile element insertion1nstd203human GRCh38 chr11: 17,937,552-17,937,552 , GRCh37.p13 chr11: 17,959,099-17,959,099 SERGEF
    nsv5183786mobile element insertion1nstd203human GRCh38 chr11: 17,836,381-17,836,399 , GRCh37.p13 chr11: 17,857,928-17,857,946 SERGEF
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