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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098462copy number variation1nstd102humanPathogenic GRCh37 chr9: 3,828,272-5,126,791 , GRCh38.p12 chr9: 3,828,272-5,126,791 AK3, TCF3P1, 30 more genes
    nsv7073649inversion1nstd229human GRCh38 chr9: 4,659,571-5,011,425 , GRCh37.p13 chr9: 4,659,571-5,011,425 RCL1, CDC37L1, 11 more genes
    nsv7066230inversion1nstd229human GRCh38 chr9: 235,930-9,843,002 , GRCh37.p13 chr9: 235,930-9,843,002 GLIS3-AS1, LOC105375955, 118 more genes
    nsv6876223copy number variation1nstd229human GRCh38 chr9: 4,683,363-4,687,946 , GRCh37.p13 chr9: 4,683,363-4,687,946 CDC37L1
    nsv6873097copy number variation1nstd229human GRCh38 chr9: 4,664,051-4,822,692 , GRCh37.p13 chr9: 4,664,051-4,822,692 CDC37L1-DT, RCL1, 7 more genes
    nsv6869706copy number variation1nstd229human GRCh38 chr9: 4,065,650-4,678,397 , GRCh37.p13 chr9: 4,065,650-4,678,397 RNU6-694P, SPATA6L, 7 more genes
    nsv6869284copy number variation1nstd229human GRCh38 chr9: 4,625,106-4,732,095 , GRCh37.p13 chr9: 4,625,106-4,732,095 AK3, CDC37L1, 4 more genes
    nsv6868145copy number variation1nstd229human GRCh38 chr9: 4,606,225-4,820,320 , GRCh37.p13 chr9: 4,606,225-4,820,320 CDC37L1, ECM1P1, 8 more genes
    nsv6866472copy number variation1nstd229human GRCh38 chr9: 4,573,180-4,701,765 , GRCh37.p13 chr9: 4,573,180-4,701,765 SLC1A1, PLPP6, 4 more genes
    nsv6863892copy number variation1nstd229human GRCh38 chr9: 4,625,116-5,645,668 , GRCh37.p13 chr9: 4,625,116-5,645,668 INSL6, TCF3P1, 33 more genes
    nsv6862605copy number variation1nstd229human GRCh38 chr9: 4,704,675-4,704,812 , GRCh37.p13 chr9: 4,704,675-4,704,812 CDC37L1
    nsv6860473copy number variation1nstd229human GRCh38 chr9: 4,665,528-4,706,825 , GRCh37.p13 chr9: 4,665,528-4,706,825 CDC37L1, CDC37L1-DT, 2 more genes
    nsv6638036copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 203,862-5,958,840 , GRCh38.p12 chr9: 203,862-5,958,840 DMRT1, MLANA, 86 more genes
    nsv6637634copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,386,288-5,003,101 , GRCh38.p12 chr9: 4,386,288-5,003,101 MIR101-2, PLPP6, 14 more genes
    nsv6637297copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,604,171-5,491,331 , GRCh38.p12 chr9: 4,604,171-5,491,331 KLF4P1, HNRNPA1P41, 31 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634450copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-15,048,247 , GRCh38.p12 chr9: 203,861-15,048,249 LOC102724027, DMRT2, 157 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6562193inversion1nstd223human GRCh38 chr9: 4,534,449-5,089,056 , GRCh37.p13 chr9: 4,534,449-5,089,056 PLPP6, AK3, 15 more genes
    nsv6556011inversion1nstd223human GRCh38 chr9: 4,687,665-4,688,007 , GRCh37.p13 chr9: 4,687,665-4,688,007 CDC37L1
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