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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3871156copy number variation1nstd102humanBenign GRCh37 chr2: 38,280,021-38,303,019 , GRCh38.p12 chr2: 38,052,878-38,075,877 RMDN2, CYP1B1
    nsv3886682copy number variation1nstd102humanBenign GRCh37 chr2: 38,096,272-38,212,781 , GRCh38.p12 chr2: 37,869,129-37,985,638 RMDN2, RMDN2-AS1, 1 more genes
    nsv3886628copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,092,623-38,340,684 , GRCh38.p12 chr2: 37,865,480-38,113,542 RMDN2, PIRAT1, 3 more genes
    nsv3884418copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,232,794-38,359,795 , GRCh38.p12 chr2: 38,005,651-38,132,653 RMDN2, RMDN2-AS1, 3 more genes
    nsv3889073copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,206,638-38,332,303 , GRCh38.p12 chr2: 37,979,495-38,105,161 RMDN2, RMDN2-AS1, 2 more genes
    nsv4454718copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,291,099-38,373,417 , GRCh38.p12 chr2: 38,063,956-38,146,275 RMDN2, LOC107985871, 3 more genes
    nsv4449864copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,291,099-38,359,165 , GRCh38.p12 chr2: 38,063,956-38,132,023 RMDN2, CYP1B1-AS1, 1 more genes
    nsv4674626copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,059,333-38,261,030 , GRCh38.p12 chr2: 37,832,190-38,033,887 RMDN2, PIRAT1, 2 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 RMDN2, CYP1B1-AS1, 1649 more genes
    nsv6313619copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300 RMDN2, LOC107985870, 161 more genes
    nsv3899050copy number variation1nstd102humanPathogenic NCBI36 chr2: 37,081,204-42,035,330 , GRCh37 chr2: 37,227,700-42,181,826 , GRCh38 chr2: 37,000,557-41,954,686 RMDN2, LOC375196, 78 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 RMDN2, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 RMDN2, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RMDN2, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 RMDN2, 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 RMDN2, SLC35F6, 801 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 RMDN2, ALLC, 674 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 RMDN2, RPL7P13, 426 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 RMDN2, ATL2, 465 more genes
    nsv3882842copy number variation1nstd102humanPathogenic GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406 RMDN2, STON1, 303 more genes
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