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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979667inversion1nstd209human GRCh38 chr13: 24,646,334-25,024,564 , GRCh37.p13 chr13: 25,220,472-25,598,702 , ATP12A, 14 more genes
    nsv5974315insertion1nstd209human GRCh38 chr13: 24,882,090-24,882,090 , GRCh37.p13 chr13: 25,456,228-25,456,228 CENPJ, RNF17
    nsv5944008copy number variation1nstd209human GRCh38 chr13: 24,899,983-24,900,168 , GRCh37.p13 chr13: 25,474,121-25,474,306 CENPJ
    nsv5934708copy number variation1nstd209human GRCh38 chr13: 24,882,153-24,882,212 , GRCh37.p13 chr13: 25,456,291-25,456,350 RNF17, CENPJ
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    nsv5662994insertion1nstd207human GRCh38 chr13: 24,881,827-24,881,827 , GRCh37.p13 chr13: 25,455,965-25,455,965 RNF17, CENPJ
    nsv5662031insertion1nstd207human GRCh38 chr13: 24,882,089-24,882,089 , GRCh37.p13 chr13: 25,456,227-25,456,227 CENPJ, RNF17
    nsv5653689insertion1nstd207human GRCh38 chr13: 24,882,101-24,882,101 , GRCh37.p13 chr13: 25,456,239-25,456,239 RNF17, CENPJ
    nsv5653546insertion1nstd207human GRCh38 chr13: 24,881,964-24,881,964 , GRCh37.p13 chr13: 25,456,102-25,456,102 CENPJ, RNF17
    nsv5652520insertion1nstd207human GRCh38 chr13: 24,882,211-24,882,211 , GRCh37.p13 chr13: 25,456,349-25,456,349 CENPJ, RNF17
    nsv5651766insertion1nstd207human GRCh38 chr13: 24,881,871-24,881,871 , GRCh37.p13 chr13: 25,456,009-25,456,009 RNF17, CENPJ
    nsv5645961insertion1nstd207human GRCh38 chr13: 24,882,183-24,882,183 , GRCh37.p13 chr13: 25,456,321-25,456,321 RNF17, CENPJ
    nsv5644532insertion1nstd207human GRCh38 chr13: 24,881,962-24,881,962 , GRCh37.p13 chr13: 25,456,100-25,456,100 CENPJ, RNF17
    nsv5596210copy number variation1nstd207human GRCh38 chr13: 24,882,129-24,882,232 , GRCh37.p13 chr13: 25,456,267-25,456,370 RNF17, CENPJ
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561491sequence alteration1nstd206human GRCh38 chr13: 24,595,804-24,953,333 , GRCh37.p13 chr13: 25,169,942-25,527,471 , ATP12A, 13 more genes
    nsv5504351copy number variation1nstd206human GRCh38 chr13: 24,891,179-24,892,135 , GRCh37.p13 chr13: 25,465,317-25,466,273 CENPJ
    nsv5503803copy number variation1nstd206human GRCh38 chr13: 24,899,986-24,900,169 , GRCh37.p13 chr13: 25,474,124-25,474,307 CENPJ
    nsv5343707translocation1nstd200human GRCh37 chr13: 25,474,307-25,474,307 , GRCh37 chr13: 25,474,124-25,474,124 , GRCh38.p12 chr13: 24,900,169-24,900,169 , GRCh38.p12 chr13: 24,899,986-24,899,986 CENPJ
    nsv5319807copy number variation1nstd204human GRCh38.p13 chr13: 24,899,977-24,900,177 , GRCh37.p13 chr13: 25,474,115-25,474,315 CENPJ
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