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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065747inversion1nstd229human GRCh38 chr11: 5,811,210-5,821,063 , GRCh37.p13 chr11: 5,832,440-5,842,293 OR52N2
    nsv6917036copy number variation1nstd229human GRCh38 chr11: 5,803,500-5,803,985 , GRCh37.p13 chr11: 5,824,730-5,825,215 OR52N2
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6913212copy number variation1nstd229human GRCh38 chr11: 5,742,188-5,844,344 , GRCh37.p13 chr11: 5,763,418-5,865,574 OR56B2P, OR52N3P, 5 more genes
    nsv6913006copy number variation1nstd229human GRCh38 chr11: 5,808,285-5,808,342 , GRCh37.p13 chr11: 5,829,515-5,829,572 OR52N2
    nsv6912427copy number variation1nstd229human GRCh38 chr11: 5,815,794-5,820,812 , GRCh37.p13 chr11: 5,837,024-5,842,042 OR52N2
    nsv6902633copy number variation1nstd229human GRCh38 chr11: 5,538,086-5,938,396 , GRCh37.p13 chr11: 5,559,316-5,959,626 OR52N1, OR52N4, 26 more genes
    nsv6901512copy number variation1nstd229human GRCh38 chr11: 5,821,119-5,823,333 , GRCh37.p13 chr11: 5,842,349-5,844,563 OR52N2
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6621251copy number variation1nstd224human GRCh37 chr11: 5,727,822-5,995,159 , GRCh38.p12 chr11: 5,706,592-5,973,929 TRIM22, OR52N1, 17 more genes
    nsv6590262inversion1nstd223human GRCh38 chr11: 5,786,169-5,868,284 , GRCh37.p13 chr11: 5,807,399-5,889,514 OR52N1, OR52N3P, 3 more genes
    nsv6445684copy number variation1nstd223human GRCh38 chr11: 5,783,536-5,827,474 , GRCh37.p13 chr11: 5,804,766-5,848,704 OR52N2, OR52N1, 1 more genes
    nsv6441849copy number variation1nstd223human GRCh38 chr11: 5,588,812-6,011,442 , GRCh37.p13 chr11: 5,610,042-6,032,672 OR52N5, OR52N4, 26 more genes
    nsv6440896copy number variation1nstd223human GRCh38 chr11: 5,810,801-5,811,600 , GRCh37.p13 chr11: 5,832,031-5,832,830 OR52N2
    nsv6437487copy number variation1nstd223human GRCh38 chr11: 5,568,264-6,075,481 , GRCh37.p13 chr11: 5,589,494-6,096,711 TRIM34, OR52E6, 33 more genes
    nsv6436757copy number variation1nstd223human GRCh38 chr11: 5,618,722-5,835,186 , GRCh37.p13 chr11: 5,639,952-5,856,416 OR56B2P, OR52P1, 12 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6293466mobile element insertion1nstd186human GRCh37 chr11: 5,842,604-5,842,655 , GRCh38.p12 chr11: 5,821,374-5,821,425 OR52N2
    nsv6191693copy number variation1nstd214human GRCh38 chr11: 5,808,285-5,808,341 , GRCh37.p13 chr11: 5,829,515-5,829,571 OR52N2
    nsv6025966copy number variation1nstd212human GRCh38 chr11: 5,808,296-5,808,353 , GRCh37.p13 chr11: 5,829,526-5,829,583 OR52N2
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