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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065616inversion1nstd229human GRCh38 chr11: 55,877,934-56,853,091 , GRCh37.p13 chr11: 55,645,410-56,620,567 OR5M5P, OR5G3, 74 more genes
    nsv6917693copy number variation1nstd229human GRCh38 chr11: 56,149,374-56,499,735 , GRCh37.p13 chr11: 55,916,850-56,267,211 NAA50P1, OR5M7P, 27 more genes
    nsv6914832copy number variation1nstd229human GRCh38 chr11: 56,255,139-56,525,470 , GRCh37.p13 chr11: 56,022,615-56,292,946 OR5M3, OR8U3, 22 more genes
    nsv6911180copy number variation1nstd229human GRCh38 chr11: 56,483,334-56,512,980 , GRCh37.p13 chr11: 56,250,810-56,280,456 OR5M8, OR5M7P, 3 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
    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
    nsv6903036copy number variation1nstd229human GRCh38 chr11: 56,420,634-56,537,480 , GRCh37.p13 chr11: 56,188,110-56,304,956 OR5M6P, OR5M4P, 8 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
    nsv6475397copy number variation1nstd223human GRCh38 chr11: 56,149,374-56,499,735 , GRCh37.p13 chr11: 55,916,850-56,267,211 OR8H1, OR8K5, 27 more genes
    nsv6473471copy number variation1nstd223human GRCh38 chr11: 56,491,102-56,501,100 , GRCh37.p13 chr11: 56,258,578-56,268,576 LOC100128210, OR5M8, 1 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
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5967593inversion1nstd209human GRCh37.p13 chr11: 56,237,631-56,258,841 , GRCh38 chr11: 56,470,155-56,491,365 OR5M2P, OR5M3, 1 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
    nsv5911995copy number variation1nstd209human GRCh38 chr11: 56,491,750-56,492,406 , GRCh37.p13 chr11: 56,259,226-56,259,882 OR5M8
    nsv5501377copy number variation1nstd206human GRCh38 chr11: 56,489,285-56,489,468 , GRCh37.p13 chr11: 56,256,761-56,256,944 OR5M8
    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
    nsv4984955copy number variation1nstd200human GRCh38 chr11: 56,491,058-56,501,153 , GRCh37.p13 chr11: 56,258,534-56,268,629 LOC100128210, OR5M7P, 1 more genes
    nsv4839337copy number variation1nstd200human GRCh37 chr11: 56,258,534-56,268,629 , GRCh38.p12 chr11: 56,491,058-56,501,153 OR5M8, OR5M7P, 1 more genes
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