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Items: 1 to 20 of 218

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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
    nsv7097727copy number variation1nstd102humanUncertain significance GRCh37 chr9: 37,422,744-37,436,779 , GRCh38.p12 chr9: 37,422,747-37,436,782 CHCHD4P3, ZBTB5, 1 more genes
    nsv7077787inversion1nstd229human GRCh38 chr9: 36,095,897-37,616,085 , GRCh37.p13 chr9: 36,095,894-37,616,082 RPL21P83, MRPS21P4, 33 more genes
    nsv7072573inversion1nstd229human GRCh38 chr9: 37,202,331-37,505,813 , GRCh37.p13 chr9: 37,202,328-37,505,810 POLR1E, GRHPR, 8 more genes
    nsv7068279inversion1nstd229human GRCh38 chr9: 36,238,268-37,822,344 , GRCh37.p13 chr9: 36,238,265-37,822,341 MIR4540, GNE, 35 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
    nsv6876191copy number variation1nstd229human GRCh38 chr9: 37,448,922-37,448,984 , GRCh37.p13 chr9: 37,448,919-37,448,981 ZBTB5
    nsv6870922copy number variation1nstd229human GRCh38 chr9: 37,445,503-37,452,146 , GRCh37.p13 chr9: 37,445,500-37,452,143 ZBTB5
    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
    nsv6566024inversion1nstd223human GRCh38 chr9: 36,238,303-37,822,343 , GRCh37.p13 chr9: 36,238,300-37,822,340 POLR1E, LOC105376031, 35 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6315486copy number variation1nstd102humanUncertain significance GRCh37 chr9: 37,313,084-37,716,205 , GRCh38.p12 chr9: 37,313,087-37,716,208 ZBTB5, RN7SKP171, 13 more genes
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6312935copy number variation1nstd102humanPathogenic GRCh37 chr9: 37,436,648-37,436,789 , GRCh38.p12 chr9: 37,436,651-37,436,792 ZBTB5, GRHPR
    nsv6302404copy number variation1nstd186human GRCh37 chr9: 37,445,500-37,452,141 , GRCh38.p12 chr9: 37,445,503-37,452,144 ZBTB5
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