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Items: 1 to 20 of 277

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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
    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
    nsv5939560copy number variation1nstd209human GRCh38 chr13: 23,896,662-23,896,711 , GRCh37.p13 chr13: 24,470,801-24,470,850 C1QTNF9B
    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
    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
    nsv5507635copy number variation1nstd206human GRCh38 chr13: 22,700,106-24,442,106 , GRCh37.p13 chr13: 23,274,245-25,016,244 , SGCG, 40 more genes
    nsv5274467copy number variation1nstd204human GRCh38.p13 chr13: 23,876,452-23,900,767 , GRCh37.p13 chr13: 24,450,591-24,474,906 PCOTH, C1QTNF9B, 1 more genes
    nsv5269503copy number variation1nstd204human GRCh38.p13 chr13: 23,890,701-23,891,600 , GRCh37.p13 chr13: 24,464,840-24,465,739 C1QTNF9B, PCOTH
    nsv5004395copy number variation1nstd200human GRCh38 chr13: 22,932,446-24,354,679 , GRCh37.p13 chr13: 23,506,585-24,928,817 , NUS1P3, 30 more genes
    nsv4996581copy number variation1nstd200human GRCh38 chr13: 23,646,614-23,919,003 , GRCh37.p13 chr13: 24,220,753-24,493,142 , MIPEP, 6 more genes
    nsv4769365copy number variation1nstd102humanUncertain significance GRCh37 chr13: 22,423,865-25,504,992 , GRCh38.p12 chr13: 21,849,726-24,930,854 LOC105370111, DDX39AP1, 63 more genes
    nsv4729520copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 23,775,339-30,534,624 , GRCh38.p12 chr13: 23,201,200-29,960,487 PARP4, ATP12A, 136 more genes
    nsv4728116copy number variation1nstd197human GRCh38.p12 chr13: 23,894,140-23,894,201 , GRCh37 chr13: 24,468,279-24,468,340 C1QTNF9B
    nsv4680752copy number variation1nstd189human GRCh37.p13 chr13: 23,535,943-24,961,638 , GRCh38.p12 chr13: 22,961,804-24,387,500 , MIPEP, 30 more genes
    nsv4680248copy number variation1nstd189human GRCh37.p13 chr13: 23,535,943-24,948,127 , GRCh38.p12 chr13: 22,961,804-24,373,989 , MIPEP, 30 more genes
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