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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139965insertion1nstd232human GRCh37.p13 chr11: 59,344,498-59,344,498 , GRCh38.p12 chr11: 59,577,025-59,577,025 OSBP
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7066760inversion1nstd229human GRCh38 chr11: 59,609,994-59,610,131 , GRCh37.p13 chr11: 59,377,467-59,377,604 OSBP
    nsv7061712inversion1nstd229human GRCh38 chr11: 59,503,799-59,574,181 , GRCh37.p13 chr11: 59,271,272-59,341,654 TRV-TAC2-1, LOC102723575, 13 more genes
    nsv6913064copy number variation1nstd229human GRCh38 chr11: 59,433,230-59,577,351 , GRCh37.p13 chr11: 59,200,703-59,344,824 OR4D9, LINC02739, 17 more genes
    nsv6911082copy number variation1nstd229human GRCh38 chr11: 59,570,139-59,574,491 , GRCh37.p13 chr11: 59,337,612-59,341,964 OSBP
    nsv6910668copy number variation1nstd229human GRCh38 chr11: 59,589,958-59,592,930 , GRCh37.p13 chr11: 59,357,431-59,360,403 OSBP
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6900247copy number variation1nstd229human GRCh38 chr11: 59,583,049-59,584,331 , GRCh37.p13 chr11: 59,350,522-59,351,804 OSBP
    nsv6898490copy number variation1nstd229human GRCh38 chr11: 59,577,393-59,577,496 , GRCh37.p13 chr11: 59,344,866-59,344,969 OSBP
    nsv6584232inversion1nstd223human GRCh38 chr11: 59,605,041-59,605,676 , GRCh37.p13 chr11: 59,372,514-59,373,149 OSBP
    nsv6581514inversion1nstd223human GRCh38 chr11: 59,583,157-59,583,634 , GRCh37.p13 chr11: 59,350,630-59,351,107 OSBP
    nsv6578150inversion1nstd223human GRCh38 chr11: 59,603,617-59,604,554 , GRCh37.p13 chr11: 59,371,090-59,372,027 OSBP
    nsv6474088copy number variation1nstd223human GRCh38 chr11: 59,583,827-59,585,533 , GRCh37.p13 chr11: 59,351,300-59,353,006 OSBP
    nsv6471010copy number variation1nstd223human GRCh38 chr11: 59,587,325-59,588,274 , GRCh37.p13 chr11: 59,354,798-59,355,747 OSBP
    nsv6467543copy number variation1nstd223human GRCh38 chr11: 59,591,810-59,592,987 , GRCh37.p13 chr11: 59,359,283-59,360,460 OSBP
    nsv6463306copy number variation1nstd223human GRCh38 chr11: 59,613,501-59,620,300 , GRCh37.p13 chr11: 59,380,974-59,387,773 OSBP, LOC101927226
    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
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