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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093994copy number variation1nstd102humanPathogenic GRCh37 chr13: 24,293,859-26,594,123 , GRCh38.p12 chr13: 23,719,720-26,019,985 IRX1P1, MTCO3P2, 54 more genes
    nsv7063835inversion1nstd229human GRCh38 chr13: 22,751,036-26,757,157 , GRCh37.p13 chr13: 23,325,175-27,331,294 SPATA13, LOC105370122, 86 more genes
    nsv6935604copy number variation1nstd229human GRCh38 chr13: 25,173,023-25,173,650 , GRCh37.p13 chr13: 25,747,161-25,747,788 LINC00463
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6581943inversion1nstd223human GRCh38 chr13: 25,014,412-26,066,804 , GRCh37.p13 chr13: 25,588,550-26,640,942 ATP8A2, LINC00463, 18 more genes
    nsv6577502inversion1nstd223human GRCh38 chr13: 25,014,167-26,066,860 , GRCh37.p13 chr13: 25,588,305-26,640,998 LSP1P1, LOC100133284, 18 more genes
    nsv6487352copy number variation1nstd223human GRCh38 chr13: 25,170,001-25,172,400 , GRCh37.p13 chr13: 25,744,139-25,746,538 AMER2, LINC00463
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132473copy number variation1nstd213human GRCh37 chr13: 25,320,000-25,940,001 , GRCh38.p12 chr13: 24,745,862-25,365,863 PABPC3, MTMR6, 19 more genes
    nsv6132472copy number variation1nstd213human GRCh37 chr13: 24,340,000-26,020,001 , GRCh38.p12 chr13: 23,765,861-25,445,863 PABPC3, MTMR6, 49 more genes
    nsv5975068inversion1nstd209human GRCh38 chr13: 24,966,165-25,349,536 , GRCh37.p13 chr13: 25,540,303-25,923,674 PABPC3, MTMR6, 12 more genes
    nsv5974508inversion1nstd209human GRCh38 chr13: 24,952,930-25,309,954 , GRCh37.p13 chr13: 25,527,068-25,884,092 PABPC3, MTMR6, 12 more genes
    nsv5652768insertion1nstd207human GRCh38 chr13: 25,174,780-25,174,780 , GRCh37.p13 chr13: 25,748,918-25,748,918 LINC00463
    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
    nsv5553040insertion1nstd206human GRCh38 chr13: 25,174,854-25,174,875 , GRCh37.p13 chr13: 25,748,992-25,749,013 LINC00463
    nsv5534402insertion1nstd206human GRCh38 chr13: 25,174,850-25,174,858 , GRCh37.p13 chr13: 25,748,988-25,748,996 LINC00463
    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
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