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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899523copy number variation1nstd209human GRCh38 chr6: 13,587,088-13,587,168 , GRCh37.p13 chr6: 13,587,320-13,587,400 SIRT5
    nsv5844384copy number variation1nstd209human GRCh38 chr6: 13,589,195-13,590,194 , GRCh37.p13 chr6: 13,589,427-13,590,426 SIRT5
    nsv5576581copy number variation1nstd207human GRCh38 chr6: 13,587,088-13,587,168 , GRCh37.p13 chr6: 13,587,320-13,587,400 SIRT5
    nsv5469925copy number variation1nstd206human GRCh38 chr6: 13,590,455-13,590,934 , GRCh37.p13 chr6: 13,590,687-13,591,166 SIRT5
    nsv5466612copy number variation1nstd206human GRCh38 chr6: 13,524,856-13,607,768 , GRCh37.p13 chr6: 13,525,088-13,608,000 SIRT5, LOC105374938, 2 more genes
    nsv5458635copy number variation1nstd206human GRCh38 chr6: 13,587,089-13,587,169 , GRCh37.p13 chr6: 13,587,321-13,587,401 SIRT5
    nsv5309967copy number variation1nstd204human GRCh38.p13 chr6: 13,587,080-13,587,174 , GRCh37.p13 chr6: 13,587,312-13,587,406 SIRT5
    nsv5093325mobile element insertion1nstd203human GRCh38 chr6: 13,605,973-13,605,986 , GRCh37.p13 chr6: 13,606,205-13,606,218 LOC105374938, SIRT5
    nsv4652627copy number variation1nstd186human GRCh37 chr6: 13,587,321-13,587,401 , GRCh38.p12 chr6: 13,587,089-13,587,169 SIRT5
    nsv4591976copy number variation1nstd183human GRCh37 chr6: 13,574,839-13,574,972 , GRCh38.p12 chr6: 13,574,607-13,574,740 LOC105374937, SIRT5
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv4324882inversion1nstd166human GRCh37.p13 chr6: 11,087,007-14,472,606 , GRCh38.p12 chr6: 11,086,774-14,472,375 , HIVEP1, 56 more genes
    nsv4125963copy number variation1nstd166human GRCh37.p13 chr6: 13,581,153-13,592,287 , GRCh38.p12 chr6: 13,580,921-13,592,055 SIRT5
    nsv4124182copy number variation1nstd166human GRCh37.p13 chr6: 13,591,007-13,591,088 , GRCh38.p12 chr6: 13,590,775-13,590,856 SIRT5
    nsv4120259copy number variation1nstd166human GRCh37.p13 chr6: 13,558,937-13,575,704 , GRCh38.p12 chr6: 13,558,705-13,575,472 SIRT5, LOC105374937
    nsv4117615copy number variation1nstd166human GRCh37.p13 chr6: 13,587,321-13,587,401 , GRCh38.p12 chr6: 13,587,089-13,587,169 SIRT5
    nsv4114313copy number variation1nstd166human GRCh37.p13 chr6: 13,577,189-13,577,357 , GRCh38.p12 chr6: 13,576,957-13,577,125 SIRT5
    nsv3924426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,232,627-13,805,381 , GRCh38 chr6: 13,232,395-13,805,149 , NCBI36 chr6: 13,340,606-13,913,360 LOC105374936, RN7SKP204, 12 more genes
    nsv3922594copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,311,751-16,295,791 , GRCh38 chr6: 13,311,519-16,295,560 , NCBI36 chr6: 13,419,730-16,403,770 LOC107986571, LOC105374947, 47 more genes
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