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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925670copy number variation1nstd209human GRCh38 chr9: 137,436,339-137,436,390 , GRCh37.p13 chr9: 140,330,791-140,330,842 ENTPD8
    nsv5640595insertion1nstd207human GRCh38 chr9: 137,441,074-137,441,074 , GRCh37.p13 chr9: 140,335,526-140,335,526 ENTPD8
    nsv5631272insertion1nstd207human GRCh38 chr9: 137,440,910-137,440,910 , GRCh37.p13 chr9: 140,335,362-140,335,362 ENTPD8
    nsv5629084insertion1nstd207human GRCh38 chr9: 137,441,019-137,441,019 , GRCh37.p13 chr9: 140,335,471-140,335,471 ENTPD8
    nsv5625171insertion1nstd207human GRCh38 chr9: 137,436,339-137,436,339 , GRCh37.p13 chr9: 140,330,791-140,330,791 ENTPD8
    nsv5599887copy number variation1nstd207human GRCh38 chr9: 137,440,009-137,440,080 , GRCh37.p13 chr9: 140,334,461-140,334,532 ENTPD8
    nsv5598253copy number variation1nstd207human GRCh38 chr9: 137,440,892-137,441,054 , GRCh37.p13 chr9: 140,335,344-140,335,506 ENTPD8
    nsv5597776copy number variation1nstd207human GRCh38 chr9: 137,441,009-137,441,064 , GRCh37.p13 chr9: 140,335,461-140,335,516 ENTPD8
    nsv5597170copy number variation1nstd207human GRCh38 chr9: 137,440,410-137,441,054 , GRCh37.p13 chr9: 140,334,862-140,335,506 ENTPD8
    nsv5589278copy number variation1nstd207human GRCh38 chr9: 137,436,391-137,436,442 , GRCh37.p13 chr9: 140,330,843-140,330,894 ENTPD8
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv4973408copy number variation1nstd200human GRCh38 chr9: 137,436,350-137,436,499 , GRCh37.p13 chr9: 140,330,802-140,330,951 ENTPD8
    nsv4829964copy number variation1nstd200human GRCh37 chr9: 140,304,484-140,348,716 , GRCh38.p12 chr9: 137,410,032-137,454,264 NSMF, MIR7114, 3 more genes
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4742916copy number variation1nstd199human GRCh37 chr9: 140,330,807-140,330,861 , GRCh38.p12 chr9: 137,436,355-137,436,409 ENTPD8
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683512copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,033,919-140,729,425 , GRCh38.p12 chr9: 137,139,467-137,834,973 CIMIP2A, ENTPD8, 34 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 DPP7, MIR4673, 112 more genes
    nsv4668107copy number variation1nstd186human GRCh37 chr9: 140,327,529-140,333,478 , GRCh38.p12 chr9: 137,433,077-137,439,026 ENTPD8, NOXA1
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