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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674129copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,365,531-55,475,705 , GRCh38.p12 chr2: 55,138,395-55,248,569 MTIF2, CLHC1, 2 more genes
    nsv6290433copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,365,532-55,475,705 , GRCh38.p12 chr2: 55,138,396-55,248,569 MTIF2, CLHC1, 2 more genes
    nsv7096515copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,459,961-55,646,215 , GRCh38.p12 chr2: 55,232,825-55,419,079 MTIF2, PRORSD1P, 3 more genes
    nsv7096893copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,459,961-55,616,042 , GRCh38.p12 chr2: 55,232,825-55,388,906 MTIF2, CCDC88A, 3 more genes
    nsv7096669copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,459,961-55,566,804 , GRCh38.p12 chr2: 55,232,825-55,339,668 MTIF2, RPS27A, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 MTIF2, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 MTIF2, CYP1B1-AS1, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 MTIF2, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 MTIF2, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 MTIF2, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTIF2, MTND2P22, 3724 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 MTIF2, SLC35F6, 801 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 MTIF2, NAGK, 595 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 MTIF2, RPL7P13, 426 more genes
    nsv3882842copy number variation1nstd102humanPathogenic GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406 MTIF2, STON1, 303 more genes
    nsv3905626copy number variation1nstd102humanPathogenic GRCh37 chr2: 40,965,422-58,090,956 , GRCh38 chr2: 40,738,282-57,863,821 , NCBI36 chr2: 40,818,926-57,944,460 MTIF2, RNU6-433P, 220 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 MTIF2, ACTG2, 1713 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 MTIF2, LOC101927723, 1246 more genes
    nsv4450701copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,378,531-55,640,033 , GRCh38.p12 chr2: 55,151,395-55,412,897 MTIF2, RPS27A, 4 more genes
    nsv6636494copy number variation1nstd102humanUncertain significance GRCh37 chr2: 55,393,367-55,627,759 , GRCh38.p12 chr2: 55,166,231-55,400,623 MTIF2, CCDC88A, 4 more genes
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