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Items: 1 to 20 of 446

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145641insertion1nstd232human GRCh37.p13 chr9: 37,638,047-37,638,047 , GRCh38.p12 chr9: 37,638,050-37,638,050 FRMPD1
    nsv7139561insertion1nstd232human GRCh37.p13 chr9: 37,638,005-37,638,005 , GRCh38.p12 chr9: 37,638,008-37,638,008 FRMPD1
    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
    nsv7072391inversion1nstd229human GRCh38 chr9: 37,597,154-37,604,669 , GRCh37.p13 chr9: 37,597,151-37,604,666 FRMPD1
    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
    nsv6873275copy number variation1nstd229human GRCh38 chr9: 37,687,048-37,702,044 , GRCh37.p13 chr9: 37,687,045-37,702,041 FRMPD1
    nsv6870106copy number variation1nstd229human GRCh38 chr9: 37,747,320-37,749,992 , GRCh37.p13 chr9: 37,747,317-37,749,989 FRMPD1
    nsv6866037copy number variation1nstd229human GRCh38 chr9: 37,650,815-37,730,782 , GRCh37.p13 chr9: 37,650,812-37,730,779 RN7SKP171, FRMPD1
    nsv6865030copy number variation1nstd229human GRCh38 chr9: 37,625,998-37,626,132 , GRCh37.p13 chr9: 37,625,995-37,626,129 FRMPD1
    nsv6864080copy number variation1nstd229human GRCh38 chr9: 37,658,947-37,662,798 , GRCh37.p13 chr9: 37,658,944-37,662,795 RN7SKP171, FRMPD1
    nsv6861535copy number variation1nstd229human GRCh38 chr9: 37,746,319-37,746,978 , GRCh37.p13 chr9: 37,746,316-37,746,975 FRMPD1
    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
    nsv6574282inversion1nstd223human GRCh38 chr9: 37,737,628-37,738,348 , GRCh37.p13 chr9: 37,737,625-37,738,345 FRMPD1
    nsv6570499inversion1nstd223human GRCh38 chr9: 37,667,125-37,667,668 , GRCh37.p13 chr9: 37,667,122-37,667,665 FRMPD1
    nsv6566757inversion1nstd223human GRCh38 chr9: 37,697,957-37,698,754 , GRCh37.p13 chr9: 37,697,954-37,698,751 FRMPD1
    nsv6566024inversion1nstd223human GRCh38 chr9: 36,238,303-37,822,343 , GRCh37.p13 chr9: 36,238,300-37,822,340 POLR1E, LOC105376031, 35 more genes
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