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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978990inversion1nstd209human GRCh38 chr13: 19,387,175-24,442,537 , GRCh37.p13 chr13: 19,961,315-25,016,675 , PARP4, 111 more genes
    nsv5970142insertion1nstd209human GRCh38 chr13: 23,473,229-23,473,229 , GRCh37.p13 chr13: 24,047,368-24,047,368 LINC00327
    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
    nsv5934110copy number variation1nstd209human GRCh38 chr13: 23,483,501-23,483,832 , GRCh37.p13 chr13: 24,057,640-24,057,971 LINC00327
    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
    nsv5699820mobile element insertion2nstd211human GRCh38 chr13: 23,480,596-23,480,596 , GRCh37.p13 chr13: 24,054,735-24,054,735 LINC00327
    nsv5658573insertion1nstd207human GRCh38 chr13: 23,480,579-23,480,579 , GRCh37.p13 chr13: 24,054,718-24,054,718 LINC00327
    nsv5590960copy number variation1nstd207human GRCh38 chr13: 23,483,501-23,483,832 , GRCh37.p13 chr13: 24,057,640-24,057,971 LINC00327
    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
    nsv5548209insertion1nstd206human GRCh38 chr13: 23,473,186-23,473,186 , GRCh37.p13 chr13: 24,047,325-24,047,325 LINC00327
    nsv5507635copy number variation1nstd206human GRCh38 chr13: 22,700,106-24,442,106 , GRCh37.p13 chr13: 23,274,245-25,016,244 , SGCG, 40 more genes
    nsv5506151copy number variation1nstd206human GRCh38 chr13: 23,483,517-23,483,833 , GRCh37.p13 chr13: 24,057,656-24,057,972 LINC00327
    nsv5497864copy number variation1nstd206human GRCh38 chr13: 23,487,170-23,487,785 , GRCh37.p13 chr13: 24,061,309-24,061,924 LINC00327
    nsv5429951mobile element insertion1nstd206human GRCh38 chr13: 23,480,596-23,480,647 , GRCh37.p13 chr13: 24,054,735-24,054,786 LINC00327
    nsv5384284mobile element deletion2nstd186human GRCh37 chr13: 24,057,656-24,057,972 , GRCh38.p12 chr13: 23,483,517-23,483,833 LINC00327
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