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Items: 1 to 20 of 617

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140556copy number variation1nstd232human GRCh37.p13 chr11: 469,295-469,402 , GRCh38.p12 chr11: 469,295-469,402 PTDSS2
    nsv7137204copy number variation1nstd102humanPathogenic GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873 PKP3, RN7SL838P, 32 more genes
    nsv7072450inversion1nstd229human GRCh38 chr11: 413,084-471,727 , GRCh37.p13 chr11: 413,084-471,727 ANO9, SIGIRR, 3 more genes
    nsv7068392inversion1nstd229human GRCh38 chr11: 260,223-620,051 , GRCh37.p13 chr11: 260,223-620,051 MIR210, LMNTD2-AS1, 25 more genes
    nsv7067944inversion1nstd229human GRCh38 chr11: 288,558-695,861 , GRCh37.p13 chr11: 288,558-695,861 IRF7, TMEM80, 28 more genes
    nsv7064285inversion1nstd229human GRCh38 chr11: 394,243-446,551 , GRCh37.p13 chr11: 394,243-446,551 PKP3, SIGIRR, 4 more genes
    nsv6897931copy number variation1nstd229human GRCh38 chr11: 457,136-457,739 , GRCh37.p13 chr11: 457,136-457,739 PTDSS2
    nsv6897193copy number variation1nstd229human GRCh38 chr11: 464,426-464,476 , GRCh37.p13 chr11: 464,426-464,476 PTDSS2
    nsv6897071copy number variation1nstd229human GRCh38 chr11: 490,701-585,700 , GRCh37.p13 chr11: 490,701-585,700 MIR210HG, PTDSS2, 9 more genes
    nsv6891501copy number variation1nstd229human GRCh38 chr11: 434,722-447,601 , GRCh37.p13 chr11: 434,722-447,601 PTDSS2, LOC105376506, 2 more genes
    nsv6891053copy number variation1nstd229human GRCh38 chr11: 448,333-451,625 , GRCh37.p13 chr11: 448,333-451,625 PTDSS2
    nsv6890159copy number variation1nstd229human GRCh38 chr11: 466,954-471,706 , GRCh37.p13 chr11: 466,954-471,706 PTDSS2
    nsv6886732copy number variation1nstd229human GRCh38 chr11: 373,766-487,580 , GRCh37.p13 chr11: 373,766-487,580 PKP3, ANO9, 5 more genes
    nsv6886727copy number variation1nstd229human GRCh38 chr11: 454,945-455,050 , GRCh37.p13 chr11: 454,945-455,050 PTDSS2
    nsv6881347copy number variation1nstd229human GRCh38 chr11: 483,483-485,352 , GRCh37.p13 chr11: 483,483-485,352 PTDSS2
    nsv6879149copy number variation1nstd229human GRCh38 chr11: 488,410-488,475 , GRCh37.p13 chr11: 488,410-488,475 PTDSS2
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 more genes
    nsv6620742copy number variation1nstd224human GRCh37 chr11: 342,860-516,027 , GRCh38.p12 chr11: 342,860-516,027 RNH1, PKP3, 6 more genes
    nsv6620740copy number variation1nstd224human GRCh37 chr11: 339,943-533,357 , GRCh38.p12 chr11: 339,943-533,357 PKP3, PTDSS2, 8 more genes
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