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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4199345copy number variation1nstd166human GRCh37.p13 chr11: 56,756,662-56,756,717 , GRCh38.p12 chr11: 56,989,187-56,989,242 OR5AK2
    esv3361446copy number variation1estd59human NCBI36 chr11: 56,513,125-56,532,346 , GRCh37.p13 chr11: 56,756,549-56,775,770 , GRCh38.p12 chr11: 56,989,074-57,008,295 OR5AK2
    esv3361674copy number variation1estd59human NCBI36 chr11: 56,510,948-56,511,358 , GRCh37.p13 chr11: 56,754,372-56,754,782 , GRCh38.p12 chr11: 56,986,897-56,987,307 OR5AK2
    nsv6899622copy number variation1nstd229human GRCh38 chr11: 56,980,370-56,993,071 , GRCh37.p13 chr11: 56,747,845-56,760,546 OR5AK2
    esv2890682insertion1estd209human GRCh37 chr11: 56,755,773-56,755,773 , GRCh38.p12 chr11: 56,988,298-56,988,298 OR5AK2
    esv2080104insertion1estd194human NCBI36 chr11: 56,512,350-56,512,350 , GRCh37.p13 chr11: 56,755,774-56,755,774 , GRCh38.p12 chr11: 56,988,299-56,988,299 OR5AK2
    esv3418631copy number variation1estd59human NCBI36 chr11: 56,513,081-56,542,246 , GRCh37.p13 chr11: 56,756,505-56,785,670 , GRCh38.p12 chr11: 56,989,030-57,018,195 OR5AK1P, OR5AK2
    nsv6909689copy number variation1nstd229human GRCh38 chr11: 56,969,523-57,004,001 , GRCh37.p13 chr11: 56,736,998-56,771,476 OR5AK2, OR5AK3P
    nsv6464488copy number variation1nstd223human GRCh38 chr11: 56,969,523-57,004,001 , GRCh37.p13 chr11: 56,736,998-56,771,476 OR5AK2, OR5AK3P
    nsv5507522copy number variation1nstd206human GRCh38 chr11: 56,969,523-57,004,001 , GRCh37.p13 chr11: 56,736,998-56,771,476 OR5AK3P, OR5AK2
    nsv4984961copy number variation1nstd200human GRCh38 chr11: 56,969,523-57,004,001 , GRCh37.p13 chr11: 56,736,998-56,771,476 OR5AK3P, OR5AK2
    nsv4602678copy number variation1nstd183human GRCh37 chr11: 56,739,201-56,760,426 , GRCh38.p12 chr11: 56,971,726-56,992,951 OR5AK3P, OR5AK2
    nsv3972377copy number variation1nstd102humanLikely benign GRCh37 chr11: 56,641,835-56,771,165 , GRCh38.p12 chr11: 56,874,359-57,003,690 OR5AK2, LOC105369310, 3 more genes
    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
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 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
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 more genes
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