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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074966inversion1nstd229human GRCh38 chr9: 94,196,394-94,196,477 , GRCh37.p13 chr9: 96,958,676-96,958,759 LINC02603
    nsv7061653inversion1nstd229human GRCh38 chr9: 94,052,039-94,219,346 , GRCh37.p13 chr9: 96,814,321-96,981,628 LINC02603, MIRLET7D, 4 more genes
    nsv7060088inversion1nstd229human GRCh38 chr9: 94,202,646-94,312,127 , GRCh37.p13 chr9: 96,964,928-97,074,409 ZNF169, LINC02603, 2 more genes
    nsv6876665copy number variation1nstd229human GRCh38 chr9: 94,254,833-94,261,097 , GRCh37.p13 chr9: 97,017,115-97,023,379 ZNF169, LINC02603
    nsv6876403copy number variation1nstd229human GRCh38 chr9: 94,246,549-94,248,965 , GRCh37.p13 chr9: 97,008,831-97,011,247 LINC02603
    nsv6875885copy number variation1nstd229human GRCh38 chr9: 94,224,100-94,229,428 , GRCh37.p13 chr9: 96,986,382-96,991,710 LINC02603
    nsv6874771copy number variation1nstd229human GRCh38 chr9: 94,155,149-94,174,802 , GRCh37.p13 chr9: 96,917,431-96,937,084 MIRLET7A1, LINC02603, 2 more genes
    nsv6869575copy number variation1nstd229human GRCh38 chr9: 94,238,627-94,238,671 , GRCh37.p13 chr9: 97,000,909-97,000,953 LINC02603
    nsv6869491copy number variation1nstd229human GRCh38 chr9: 94,220,664-94,225,058 , GRCh37.p13 chr9: 96,982,946-96,987,340 LINC02603
    nsv6869310copy number variation1nstd229human GRCh38 chr9: 94,236,591-94,478,286 , GRCh37.p13 chr9: 96,998,873-97,240,568 LOC105376154, LOC107987023, 8 more genes
    nsv6863044copy number variation1nstd229human GRCh38 chr9: 94,200,957-94,201,385 , GRCh37.p13 chr9: 96,963,239-96,963,667 LINC02603
    nsv6862582copy number variation1nstd229human GRCh38 chr9: 94,200,564-94,200,636 , GRCh37.p13 chr9: 96,962,846-96,962,918 LINC02603
    nsv6858499copy number variation1nstd229human GRCh38 chr9: 94,242,310-94,242,709 , GRCh37.p13 chr9: 97,004,592-97,004,991 LINC02603
    nsv6637944copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932 MIRLET7D, MIR24-1, 60 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
    nsv6633500copy number variation1nstd224human GRCh37 chr9: 96,973,995-97,228,918 , GRCh38.p12 chr9: 94,211,713-94,466,636 MFSD14B, LINC02603, 8 more genes
    nsv6575240inversion1nstd223human GRCh38 chr9: 94,247,171-94,247,433 , GRCh37.p13 chr9: 97,009,453-97,009,715 LINC02603
    nsv6568951inversion1nstd223human GRCh38 chr9: 94,253,416-94,257,886 , GRCh37.p13 chr9: 97,015,698-97,020,168 LINC02603, ZNF169
    nsv6567674inversion1nstd223human GRCh38 chr9: 94,205,001-94,206,613 , GRCh37.p13 chr9: 96,967,283-96,968,895 LINC02603
    nsv6562764inversion1nstd223human GRCh38 chr9: 94,236,597-94,237,293 , GRCh37.p13 chr9: 96,998,879-96,999,575 LINC02603
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