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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075464inversion1nstd229human GRCh38 chr11: 56,505,852-56,957,362 , GRCh37.p13 chr11: 56,273,328-56,724,837 FADS2B, TMEM230P2, 24 more genes
    nsv7065616inversion1nstd229human GRCh38 chr11: 55,877,934-56,853,091 , GRCh37.p13 chr11: 55,645,410-56,620,567 OR5M5P, OR5G3, 74 more genes
    nsv7058916inversion1nstd229human GRCh38 chr11: 56,505,855-56,960,948 , GRCh37.p13 chr11: 56,273,331-56,728,423 OR5M13P, OR5M5P, 24 more genes
    nsv6909479copy number variation1nstd229human GRCh38 chr11: 56,446,501-56,666,900 , GRCh37.p13 chr11: 56,213,977-56,434,376 OR5AM1P, OR5M2P, 17 more genes
    nsv6905961copy number variation1nstd229human GRCh38 chr11: 56,527,330-56,879,197 , GRCh37.p13 chr11: 56,294,806-56,646,673 OR5G4P, OR9G1, 20 more genes
    nsv6903817copy number variation1nstd229human GRCh38 chr11: 55,889,039-57,077,059 , GRCh37.p13 chr11: 55,656,515-56,844,534 OR5J1P, OR8H1, 83 more genes
    nsv6902197copy number variation1nstd229human GRCh38 chr11: 56,560,301-57,072,800 , GRCh37.p13 chr11: 56,327,777-56,840,275 OR5BP1P, OR5AM1P, 28 more genes
    nsv6621249copy number variation1nstd224human GRCh37 chr11: 55,171,027-56,905,911 , GRCh38.p12 chr11: 55,403,551-57,138,437 OR5I1, OR8K2P, 113 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6304731copy number variation1nstd186human GRCh37 chr11: 56,378,912-56,378,975 , GRCh38.p12 chr11: 56,611,436-56,611,499 OR5M1
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5730482mobile element insertion2nstd211human GRCh38 chr11: 56,613,563-56,613,563 , GRCh37.p13 chr11: 56,381,039-56,381,039 OR5M1
    nsv5646867insertion1nstd207human GRCh38 chr11: 56,613,563-56,613,563 , GRCh37.p13 chr11: 56,381,039-56,381,039 OR5M1
    nsv5503003copy number variation1nstd206human GRCh38 chr11: 56,611,436-56,611,499 , GRCh37.p13 chr11: 56,378,912-56,378,975 OR5M1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4680588copy number variation1nstd189human GRCh37.p13 chr11: 55,444,212-57,222,540 , GRCh38.p12 chr11: 55,676,736-57,455,067 , APLNR, 109 more genes
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