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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5478570copy number variation1nstd206human GRCh38 chr9: 3,688,656-3,695,892 , GRCh37.p13 chr9: 3,688,656-3,695,892 RFX3-DT
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5381702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,029,023-5,300,444 , GRCh38.p12 chr9: 2,029,023-5,300,444 MTND5P36, MTND2P36, 53 more genes
    nsv5256825copy number variation1nstd204human GRCh38.p13 chr9: 3,664,701-3,666,600 , GRCh37.p13 chr9: 3,664,701-3,666,600 RFX3-DT
    nsv5245799copy number variation1nstd204human GRCh38.p13 chr9: 3,663,501-3,667,300 , GRCh37.p13 chr9: 3,663,501-3,667,300 RFX3-DT
    nsv5100638mobile element insertion1nstd203human GRCh38 chr9: 3,673,705-3,673,720 , GRCh37.p13 chr9: 3,673,705-3,673,720 RFX3-DT
    nsv4969268copy number variation1nstd200human GRCh38 chr9: 3,598,985-3,803,157 , GRCh37.p13 chr9: 3,598,985-3,803,157 RFX3-DT, LOC105375962
    nsv4962991copy number variation1nstd200human GRCh38 chr9: 3,688,656-3,695,892 , GRCh37.p13 chr9: 3,688,656-3,695,892 RFX3-DT
    nsv4823071copy number variation1nstd200human GRCh37 chr9: 3,669,827-3,673,938 , GRCh38.p12 chr9: 3,669,827-3,673,938 RFX3-DT
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 DOCK8-AS1, RN7SL25P, 186 more genes
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4729343copy number variation1nstd102humanUncertain significance GRCh37 chr9: 3,321,631-3,691,150 , GRCh38.p12 chr9: 3,321,631-3,691,150 RFX3-DT, RFX3
    nsv4675646copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-14,103,730 , GRCh38.p12 chr9: 203,861-14,103,731 INSL4, LINC02851, 145 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4675043copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-14,080,419 , GRCh38.p12 chr9: 203,861-14,080,420 MTND2P36, MTND5P36, 145 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 LINC02851, LOC105375971, 184 more genes
    nsv4674896copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-10,666,419 , GRCh38.p12 chr9: 203,861-10,666,419 PDSS1P1, RNU2-25P, 120 more genes
    nsv4489334mobile element insertion1nstd166human GRCh37.p13 chr9: 3,673,702-3,673,702 , GRCh38.p12 chr9: 3,673,702-3,673,702 RFX3-DT
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