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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv7076140inversion1nstd229human GRCh38 chr9: 34,014,202-34,211,175 , GRCh37.p13 chr9: 34,014,200-34,211,173 IMPDH1P1, UBAP1, 9 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv6877555copy number variation1nstd229human GRCh38 chr9: 34,001,901-34,190,800 , GRCh37.p13 chr9: 34,001,899-34,190,798 DCAF12, RN7SKP114, 8 more genes
    nsv6876904copy number variation1nstd229human GRCh38 chr9: 34,002,001-34,210,800 , GRCh37.p13 chr9: 34,001,999-34,210,798 UBAP1, RNA5SP282, 9 more genes
    nsv6870697copy number variation1nstd229human GRCh38 chr9: 34,186,612-34,189,168 , GRCh37.p13 chr9: 34,186,610-34,189,166 LOC114224, UBAP1
    nsv6870248copy number variation1nstd229human GRCh38 chr9: 34,169,084-34,216,726 , GRCh37.p13 chr9: 34,169,082-34,216,724 RPL35AP2, RNA5SP282, 2 more genes
    nsv6870133copy number variation1nstd229human GRCh38 chr9: 34,043,094-35,876,103 , GRCh37.p13 chr9: 34,043,092-35,876,100 STOML2, ENHO, 85 more genes
    nsv6869096copy number variation1nstd229human GRCh38 chr9: 34,007,173-34,198,330 , GRCh37.p13 chr9: 34,007,171-34,198,328 DCAF12, TUBBP4, 8 more genes
    nsv6867991copy number variation1nstd229human GRCh38 chr9: 34,121,884-34,190,244 , GRCh37.p13 chr9: 34,121,882-34,190,242 IMPDH1P1, UBAP1, 3 more genes
    nsv6867507copy number variation1nstd229human GRCh38 chr9: 34,183,831-34,188,259 , GRCh37.p13 chr9: 34,183,829-34,188,257 UBAP1, LOC114224
    nsv6866046copy number variation1nstd229human GRCh38 chr9: 33,859,162-34,227,478 , GRCh37.p13 chr9: 33,859,160-34,227,476 TUBB4BP2, RPL35AP2, 15 more genes
    nsv6865658copy number variation1nstd229human GRCh38 chr9: 33,876,249-34,185,167 , GRCh37.p13 chr9: 33,876,247-34,185,165 RN7SKP114, DCAF12, 11 more genes
    nsv6865274copy number variation1nstd229human GRCh38 chr9: 34,186,988-34,198,350 , GRCh37.p13 chr9: 34,186,986-34,198,348 RPL35AP2, LOC114224, 1 more genes
    nsv6864935copy number variation1nstd229human GRCh38 chr9: 34,036,342-35,019,147 , GRCh37.p13 chr9: 34,036,340-35,019,144 SYF2P2, TUBB4BP2, 43 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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6568126inversion1nstd223human GRCh38 chr9: 34,188,430-34,189,477 , GRCh37.p13 chr9: 34,188,428-34,189,475 LOC114224, UBAP1
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