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Items: 1 to 20 of 498

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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
    nsv7077787inversion1nstd229human GRCh38 chr9: 36,095,897-37,616,085 , GRCh37.p13 chr9: 36,095,894-37,616,082 RPL21P83, MRPS21P4, 33 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
    nsv6877484copy number variation1nstd229human GRCh38 chr9: 36,636,691-36,638,976 , GRCh37.p13 chr9: 36,636,688-36,638,973 MELK
    nsv6877190copy number variation1nstd229human GRCh38 chr9: 36,564,400-36,572,943 , GRCh37.p13 chr9: 36,564,397-36,572,940 MELK
    nsv6876728copy number variation1nstd229human GRCh38 chr9: 36,357,146-36,954,849 , GRCh37.p13 chr9: 36,357,143-36,954,846 RNF38, MRPS21P4, 6 more genes
    nsv6876696copy number variation1nstd229human GRCh38 chr9: 36,568,271-36,575,111 , GRCh37.p13 chr9: 36,568,268-36,575,108 MELK
    nsv6876212copy number variation1nstd229human GRCh38 chr9: 36,598,516-36,611,417 , GRCh37.p13 chr9: 36,598,513-36,611,414 MELK
    nsv6875808copy number variation1nstd229human GRCh38 chr9: 36,569,947-36,579,308 , GRCh37.p13 chr9: 36,569,944-36,579,305 MELK
    nsv6875761copy number variation1nstd229human GRCh38 chr9: 36,623,227-36,638,980 , GRCh37.p13 chr9: 36,623,224-36,638,977 MELK
    nsv6873074copy number variation1nstd229human GRCh38 chr9: 36,646,958-36,655,150 , GRCh37.p13 chr9: 36,646,955-36,655,147 MELK
    nsv6871092copy number variation1nstd229human GRCh38 chr9: 36,462,701-36,663,400 , GRCh37.p13 chr9: 36,462,698-36,663,397 RNF38, MELK
    nsv6869785copy number variation1nstd229human GRCh38 chr9: 36,625,425-36,634,666 , GRCh37.p13 chr9: 36,625,422-36,634,663 MELK
    nsv6869723copy number variation1nstd229human GRCh38 chr9: 36,512,398-36,687,580 , GRCh37.p13 chr9: 36,512,395-36,687,577 MELK
    nsv6867993copy number variation1nstd229human GRCh38 chr9: 36,463,801-36,653,500 , GRCh37.p13 chr9: 36,463,798-36,653,497 MELK, RNF38
    nsv6867346copy number variation1nstd229human GRCh38 chr9: 36,584,036-36,592,176 , GRCh37.p13 chr9: 36,584,033-36,592,173 MELK
    nsv6867228copy number variation1nstd229human GRCh38 chr9: 36,568,346-36,589,453 , GRCh37.p13 chr9: 36,568,343-36,589,450 MELK
    nsv6862609copy number variation1nstd229human GRCh38 chr9: 36,439,501-36,663,300 , GRCh37.p13 chr9: 36,439,498-36,663,297 MELK, RNF38
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