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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2368904short tandem repeat1nstd128human GRCh37 chr5: 132,081,141-132,081,152 , GRCh38.p12 chr5: 132,745,449-132,745,460 CCNI2
    esv2488178copy number variation1estd197human NCBI36 chr5: 132,117,614-132,117,614 , GRCh37.p13 chr5: 132,089,715-132,089,715 , GRCh38.p12 chr5: 132,754,023-132,754,023 CCNI2, SEPTIN8
    esv2168966copy number variation1estd194human NCBI36 chr5: 132,117,614-132,117,615 , GRCh37.p13 chr5: 132,089,715-132,089,716 , GRCh38.p12 chr5: 132,754,023-132,754,024 CCNI2, SEPTIN8
    nsv307973copy number variation1nstd6human NCBI35 chr5: 132,117,559-132,117,561 , GRCh37.p13 chr5: 132,089,660-132,089,662 , GRCh38.p12 chr5: 132,753,968-132,753,970 CCNI2, SEPTIN8
    nsv5472195copy number variation1nstd206human GRCh38 chr5: 132,750,190-132,764,591 , GRCh37.p13 chr5: 132,085,882-132,100,283 CCNI2, SEPTIN8
    nsv3136893copy number variation1nstd151human GRCh37 chr5: 132,086,546-132,100,116 , GRCh38.p12 chr5: 132,750,854-132,764,424 CCNI2, SEPTIN8
    esv3842254copy number variation1estd219human GRCh37 chr5: 132,085,631-132,099,716 , GRCh38.p12 chr5: 132,749,939-132,764,024 CCNI2, SEPTIN8
    esv3606809copy number variation1estd214human GRCh37 chr5: 132,085,631-132,099,716 , GRCh38.p12 chr5: 132,749,939-132,764,024 CCNI2, SEPTIN8
    nsv528687copy number variation1nstd21human NCBI35 chr5: 132,113,876-132,142,746 , GRCh37.p13 chr5: 132,085,977-132,114,847 , GRCh38.p12 chr5: 132,750,285-132,779,155 CCNI2, SEPTIN8
    nsv6244854mobile element insertion1nstd215human GRCh38 chr5: 132,753,969-132,753,969 , GRCh37.p13 chr5: 132,089,661-132,089,661 CCNI2, SEPTIN8
    nsv2369011short tandem repeat3nstd128human GRCh37 chr5: 132,087,445-132,087,458 , GRCh38.p12 chr5: 132,751,753-132,751,766 CCNI2, SEPTIN8
    nsv882918copy number variation1nstd71human NCBI36 chr5: 132,046,068-132,158,923 , GRCh37.p13 chr5: 132,018,169-132,131,024 , GRCh38.p12 chr5: 132,682,477-132,795,332 CCNI2, IL4, 3 more genes
    nsv529021copy number variation1nstd21human NCBI35 chr5: 132,046,068-132,113,876 , GRCh37.p13 chr5: 132,018,169-132,085,977 , GRCh38.p12 chr5: 132,682,477-132,750,285 CCNI2, IL4, 3 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 CCNI2, MEGF10, 2080 more genes
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 CCNI2, TXNDC15, 962 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 CCNI2, LINC01023, 783 more genes
    nsv3920627copy number variation1nstd102humanPathogenic NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694 CCNI2, MIR1289-2, 138 more genes
    nsv3911932copy number variation1nstd102humanPathogenic GRCh37 chr5: 125,774,098-132,209,659 , NCBI36 chr5: 125,801,997-132,237,558 , GRCh38 chr5: 126,438,406-132,873,967 CCNI2, LOC105379176, 93 more genes
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 CCNI2, CSF2, 99 more genes
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 CCNI2, TGFBI, 110 more genes
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