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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131697mobile element insertion1nstd186human GRCh37 chr13: 24,889,022-24,889,058 , GRCh38.p12 chr13: 24,314,884-24,314,920 C1QTNF9
    nsv5978990inversion1nstd209human GRCh38 chr13: 19,387,175-24,442,537 , GRCh37.p13 chr13: 19,961,315-25,016,675 , PARP4, 111 more genes
    nsv5974070insertion1nstd209human GRCh38 chr13: 24,314,878-24,314,878 , GRCh37.p13 chr13: 24,889,016-24,889,016 C1QTNF9
    nsv5969193inversion1nstd209human GRCh38 chr13: 19,344,229-24,542,503 , GRCh37.p13 chr13: 19,918,369-25,116,641 , PARP4, 117 more genes
    nsv5943116copy number variation1nstd209human GRCh38 chr13: 22,944,712-24,366,465 , GRCh37.p13 chr13: 23,518,851-24,940,603 , NUS1P3, 30 more genes
    nsv5938299copy number variation1nstd209human GRCh38 chr13: 22,963,602-24,388,560 , GRCh37.p13 chr13: 23,537,741-24,962,698 , PCOTH, 30 more genes
    nsv5936669copy number variation1nstd209human GRCh38 chr13: 22,945,701-24,367,396 , GRCh37.p13 chr13: 23,519,840-24,941,534 , TATDN2P3, 30 more genes
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    nsv5928055copy number variation1nstd209human GRCh38 chr13: 22,936,994-24,359,921 , GRCh37.p13 chr13: 23,511,133-24,934,059 , LINC00327, 30 more genes
    nsv5927619copy number variation1nstd209human GRCh38 chr13: 22,933,611-24,355,837 , GRCh37.p13 chr13: 23,507,750-24,929,975 , ANKRD20A19P, 30 more genes
    nsv5715700mobile element insertion2nstd211human GRCh38 chr13: 24,314,884-24,314,884 , GRCh37.p13 chr13: 24,889,022-24,889,022 C1QTNF9
    nsv5648232insertion1nstd207human GRCh38 chr13: 24,314,869-24,314,869 , GRCh37.p13 chr13: 24,889,007-24,889,007 C1QTNF9
    nsv5601469copy number variation1nstd207human GRCh38 chr13: 24,308,663-24,308,752 , GRCh37.p13 chr13: 24,882,801-24,882,890 C1QTNF9
    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
    nsv5554492mobile element insertion1nstd206human GRCh38 chr13: 24,314,884-24,314,920 , GRCh37.p13 chr13: 24,889,022-24,889,058 C1QTNF9
    nsv5507635copy number variation1nstd206human GRCh38 chr13: 22,700,106-24,442,106 , GRCh37.p13 chr13: 23,274,245-25,016,244 , SGCG, 40 more genes
    nsv5501893copy number variation1nstd206human GRCh38 chr13: 24,305,199-24,305,255 , GRCh37.p13 chr13: 24,879,337-24,879,393 C1QTNF9, SPATA13
    nsv5374112translocation1nstd200human GRCh38 chr13: 24,828,292-24,828,292 , GRCh38 chr13: 24,318,726-24,318,726 , GRCh37.p13 chr13: 24,892,864-24,892,864 , GRCh37.p13 chr13: 25,402,430-25,402,430 RNF17, C1QTNF9
    nsv5340250translocation1nstd200human GRCh37 chr13: 24,892,864-24,892,864 , GRCh37 chr13: 25,402,430-25,402,430 , GRCh38.p12 chr13: 24,318,726-24,318,726 , GRCh38.p12 chr13: 24,828,292-24,828,292 RNF17, C1QTNF9
    nsv5325793translocation1nstd204human GRCh37.p13 chr13: 24,890,372-24,890,372 , GRCh37.p13 chr13: 24,876,555-24,876,555 , GRCh38.p13 chr13: 24,302,417-24,302,417 , GRCh38.p13 chr13: 24,316,234-24,316,234 SPATA13, C1QTNF9
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