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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055432inversion1nstd229human GRCh38 chr3: 178,407,350-179,923,018 , GRCh37.p13 chr3: 178,125,138-179,640,806 H3P13, ZMAT3, 20 more genes
    nsv6737326copy number variation1nstd229human GRCh38 chr3: 179,618,883-179,620,405 , GRCh37.p13 chr3: 179,336,671-179,338,193 NDUFB5
    nsv6736658copy number variation1nstd229human GRCh38 chr3: 179,624,195-179,624,221 , GRCh37.p13 chr3: 179,341,983-179,342,009 NDUFB5
    nsv6734556copy number variation1nstd229human GRCh38 chr3: 179,615,001-179,629,500 , GRCh37.p13 chr3: 179,332,789-179,347,288 NDUFB5
    nsv6734493copy number variation1nstd229human GRCh38 chr3: 179,394,501-179,680,800 , GRCh37.p13 chr3: 179,112,289-179,398,588 MFN1, ACTL6A, 7 more genes
    nsv6731317copy number variation1nstd229human GRCh38 chr3: 179,625,952-179,635,313 , GRCh37.p13 chr3: 179,343,740-179,353,101 NDUFB5
    nsv6729416copy number variation1nstd229human GRCh38 chr3: 179,625,901-179,635,300 , GRCh37.p13 chr3: 179,343,689-179,353,088 NDUFB5
    nsv6729110copy number variation1nstd229human GRCh38 chr3: 179,611,524-179,622,111 , GRCh37.p13 chr3: 179,329,312-179,339,899 NDUFB5
    nsv6719132copy number variation1nstd229human GRCh38 chr3: 179,616,201-179,741,700 , GRCh37.p13 chr3: 179,333,989-179,459,488 USP13, H3P13, 1 more genes
    nsv6634512copy number variation1nstd102humanPathogenic GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576 LOC105374243, RNF13P1, 34 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6557127inversion1nstd223human GRCh38 chr3: 179,616,242-179,617,455 , GRCh37.p13 chr3: 179,334,030-179,335,243 NDUFB5
    nsv6375470copy number variation1nstd223human GRCh38 chr3: 179,618,883-179,620,444 , GRCh37.p13 chr3: 179,336,671-179,338,232 NDUFB5
    nsv6358683copy number variation1nstd223human GRCh38 chr3: 179,626,695-179,631,858 , GRCh37.p13 chr3: 179,344,483-179,349,646 NDUFB5
    nsv6296013copy number variation1nstd186human GRCh37 chr3: 179,344,269-179,345,143 , GRCh38.p12 chr3: 179,626,481-179,627,355 NDUFB5
    nsv6293546mobile element insertion1nstd186human GRCh37 chr3: 179,330,975-179,330,975 , GRCh38.p12 chr3: 179,613,187-179,613,187 NDUFB5
    nsv6291110copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 168,118,411-179,867,071 , GRCh38.p12 chr3: 168,400,623-180,149,283 ACTL6A, ECT2, 141 more genes
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv6134795copy number variation1nstd213human GRCh37 chr3: 178,940,000-180,410,001 , GRCh38.p12 chr3: 179,222,212-180,692,213 NDUFB5, PIK3CA, 21 more genes
    nsv5904081copy number variation1nstd209human GRCh38 chr3: 179,621,419-179,621,473 , GRCh37.p13 chr3: 179,339,207-179,339,261 NDUFB5
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