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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5525130copy number variation1nstd206human GRCh38 chr15: 84,364,100-84,661,533 , GRCh37.p13 chr15: 84,938,819-85,204,764 , LOC103171574, 21 more genes
    nsv5519680copy number variation1nstd206human GRCh38 chr15: 84,659,001-84,659,572 , GRCh37.p13 chr15: 85,202,232-85,202,803 NMB
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5320769translocation1nstd204human GRCh38.p13 chr15: 84,659,572-84,659,572 , GRCh38.p13 chr15: 84,659,000-84,659,000 , GRCh37.p13 chr15: 85,202,803-85,202,803 , GRCh37.p13 chr15: 85,202,231-85,202,231 NMB
    nsv5002115copy number variation1nstd200human GRCh38 chr15: 84,659,001-84,659,572 , GRCh37.p13 chr15: 85,202,232-85,202,803 NMB
    nsv4856125copy number variation1nstd200human GRCh37 chr15: 85,202,232-85,202,805 , GRCh38.p12 chr15: 84,659,001-84,659,574 NMB
    nsv4729284copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,201,955-85,786,847 , GRCh38.p12 chr15: 82,641,775-85,243,616 GOLGA6L5P, DNM1P44, 77 more genes
    nsv4728977copy number variation1nstd102humanUncertain significance GRCh37 chr15: 85,089,553-85,876,582 , GRCh38.p12 chr15: 84,546,322-85,333,351 WDR73, CSPG4P12, 23 more genes
    nsv4675910copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 84,928,663-85,786,847 , GRCh38.p12 chr15: 84,259,911-85,243,616 NMB, PDE8A, 37 more genes
    nsv4670255copy number variation1nstd186human GRCh37 chr15: 85,202,193-85,202,778 , GRCh38.p12 chr15: 84,658,962-84,659,547 NMB
    nsv4629148copy number variation1nstd183human GRCh37 chr15: 85,202,193-85,202,778 , GRCh38.p12 chr15: 84,658,962-84,659,547 NMB
    nsv4622276copy number variation1nstd183human GRCh37 chr15: 85,077,738-85,726,714 , GRCh38.p12 chr15: 84,534,507-85,183,483 NMB, ZSCAN2, 15 more genes
    nsv4456148copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,884,801-85,724,984 , GRCh38.p12 chr15: 84,216,049-85,181,753 NMB, LOC102724117, 35 more genes
    nsv4387671copy number variation1nstd173human GRCh37 chr15: 84,827,469-85,786,847 , GRCh38.p12 chr15: 84,158,717-85,243,616 , GOLGA6L4, 47 more genes
    nsv4350274copy number variation1nstd102humanPathogenic GRCh37 chr15: 83,883,823-92,165,844 , GRCh38.p12 chr15: 83,215,071-91,622,614 AKAP13, LOC105370972, 184 more genes
    nsv4349159copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 85,147,499-85,681,120 , GRCh38.p12 chr15: 84,604,268-85,137,889 NMB, PDE8A, 12 more genes
    nsv4248913copy number variation1nstd166human GRCh37.p13 chr15: 85,180,295-85,204,963 , GRCh38.p12 chr15: 84,637,064-84,661,732 WDR73, NMB, 1 more genes
    nsv4234029copy number variation1nstd166human GRCh37.p13 chr15: 85,202,232-85,202,803 , GRCh38.p12 chr15: 84,659,001-84,659,572 NMB
    nsv3959505copy number variation1nstd168human GRCh38 chr15: 84,658,102-84,715,989 , GRCh37.p13 chr15: 85,201,333-85,259,220 NMB, SEC11A
    nsv3923818copy number variation1nstd102humanUncertain significance GRCh37 chr15: 84,946,133-85,700,902 , GRCh38 chr15: 84,391,435-85,157,671 , NCBI36 chr15: 82,737,137-83,501,906 LOC102724135, LINC00933, 28 more genes
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