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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
    nsv6876355copy number variation1nstd229human GRCh38 chr9: 4,773,300-5,092,659 , GRCh37.p13 chr9: 4,773,300-5,092,659 RCL1, PDSS1P1, 10 more genes
    nsv6874289copy number variation1nstd229human GRCh38 chr9: 4,797,901-4,814,300 , GRCh37.p13 chr9: 4,797,901-4,814,300 KLF4P1, RCL1
    nsv6874127copy number variation1nstd229human GRCh38 chr9: 4,801,559-4,806,218 , GRCh37.p13 chr9: 4,801,559-4,806,218 KLF4P1, RCL1
    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
    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
    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
    nsv6859028copy number variation1nstd229human GRCh38 chr9: 4,713,801-4,942,500 , GRCh37.p13 chr9: 4,713,801-4,942,500 MIR101-2, AK3, 5 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
    nsv6315522copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-10,283,912 , GRCh38.p12 chr9: 203,861-10,283,912 DMAC1, RNU7-185P, 119 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 more genes
    nsv6315458copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-12,570,076 , GRCh38.p12 chr9: 203,861-12,570,076 LINC02851, GLIS3, 129 more genes
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