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Items: 1 to 20 of 99

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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
    nsv6916926copy number variation1nstd229human GRCh38 chr11: 56,724,228-56,905,443 , GRCh37.p13 chr11: 56,491,704-56,672,919 LINC02735, MIR6128, 9 more genes
    nsv6912186copy number variation1nstd229human GRCh38 chr11: 56,773,522-56,777,688 , GRCh37.p13 chr11: 56,540,998-56,545,164 OR5G1P
    nsv6911706copy number variation1nstd229human GRCh38 chr11: 56,696,974-56,885,351 , GRCh37.p13 chr11: 56,464,450-56,652,827 OR9G4, OR5G1P, 8 more genes
    nsv6909594copy number variation1nstd229human GRCh38 chr11: 56,760,801-56,911,900 , GRCh37.p13 chr11: 56,528,277-56,679,376 OR5G4P, LINC02735, 5 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
    nsv6904226copy number variation1nstd229human GRCh38 chr11: 56,762,134-56,822,705 , GRCh37.p13 chr11: 56,529,610-56,590,181 OR5G3, OR5G5P, 2 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
    nsv6903755copy number variation1nstd229human GRCh38 chr11: 56,772,984-56,781,297 , GRCh37.p13 chr11: 56,540,460-56,548,773 OR5G1P
    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
    nsv6898176copy number variation1nstd229human GRCh38 chr11: 56,772,701-56,777,700 , GRCh37.p13 chr11: 56,540,177-56,545,176 OR5G1P
    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
    nsv6462977copy number variation1nstd223human GRCh38 chr11: 56,703,718-56,793,119 , GRCh37.p13 chr11: 56,471,194-56,560,595 OR9G2P, OR5G4P, 4 more genes
    nsv6458626copy number variation1nstd223human GRCh38 chr11: 56,773,522-56,777,686 , GRCh37.p13 chr11: 56,540,998-56,545,162 OR5G1P
    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
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5917077copy number variation1nstd209human GRCh38 chr11: 56,773,521-56,777,685 , GRCh37.p13 chr11: 56,540,997-56,545,161 OR5G1P
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