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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911205copy number variation1nstd209human GRCh38 chr11: 60,823,935-60,824,088 , GRCh37.p13 chr11: 60,591,408-60,591,561 LOC105369322
    nsv5910101copy number variation1nstd209human GRCh38 chr11: 60,815,407-60,815,583 , GRCh37.p13 chr11: 60,582,880-60,583,056 LOC105369322
    nsv5724994mobile element insertion2nstd211human GRCh38 chr11: 60,823,656-60,823,656 , GRCh37.p13 chr11: 60,591,129-60,591,129 LOC105369322
    nsv5599275copy number variation1nstd207human GRCh38 chr11: 60,814,900-60,815,208 , GRCh37.p13 chr11: 60,582,373-60,582,681 LOC105369322
    nsv5598797copy number variation1nstd207human GRCh38 chr11: 60,823,970-60,824,035 , GRCh37.p13 chr11: 60,591,443-60,591,508 LOC105369322
    nsv5588184copy number variation1nstd207human GRCh38 chr11: 60,815,385-60,815,561 , GRCh37.p13 chr11: 60,582,858-60,583,034 LOC105369322
    nsv5585613copy number variation1nstd207human GRCh38 chr11: 60,803,957-60,804,447 , GRCh37.p13 chr11: 60,571,430-60,571,920 LOC105369322
    nsv5508270copy number variation1nstd206human GRCh38 chr11: 60,835,717-60,836,908 , GRCh37.p13 chr11: 60,603,190-60,604,381 LOC105369322
    nsv5502264copy number variation1nstd206human GRCh38 chr11: 60,823,293-60,823,366 , GRCh37.p13 chr11: 60,590,766-60,590,839 LOC105369322
    nsv5500055copy number variation1nstd206human GRCh38 chr11: 60,813,080-60,813,212 , GRCh37.p13 chr11: 60,580,553-60,580,685 LOC105369322
    nsv5497467copy number variation1nstd206human GRCh38 chr11: 60,805,107-60,806,923 , GRCh37.p13 chr11: 60,572,580-60,574,396 LOC105369322
    nsv5390235copy number variation1nstd186human GRCh37 chr11: 60,571,416-60,571,921 , GRCh38.p12 chr11: 60,803,943-60,804,448 LOC105369322
    nsv5389565copy number variation1nstd186human GRCh37 chr11: 60,571,522-60,571,755 , GRCh38.p12 chr11: 60,804,049-60,804,282 LOC105369322
    nsv5382134mobile element deletion1nstd186human GRCh37 chr11: 60,571,410-60,571,721 , GRCh38.p12 chr11: 60,803,937-60,804,248 LOC105369322
    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
    nsv5355243translocation1nstd200human GRCh38 chr11: 60,805,107-60,805,107 , GRCh38 chr11: 60,806,923-60,806,923 , GRCh37.p13 chr11: 60,574,396-60,574,396 , GRCh37.p13 chr11: 60,572,580-60,572,580 LOC105369322
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv5315738copy number variation1nstd204human GRCh38.p13 chr11: 60,804,048-60,804,426 , GRCh37.p13 chr11: 60,571,521-60,571,899 LOC105369322
    nsv5314536copy number variation1nstd204human GRCh38.p13 chr11: 60,804,019-60,804,311 , GRCh37.p13 chr11: 60,571,492-60,571,784 LOC105369322
    nsv5310033copy number variation1nstd204human GRCh38.p13 chr11: 60,813,074-60,813,217 , GRCh37.p13 chr11: 60,580,547-60,580,690 LOC105369322
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