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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880961copy number variation1nstd102humanBenign GRCh37 chr2: 44,445,686-44,467,993 , GRCh38.p12 chr2: 44,218,547-44,240,854 PPM1B
    nsv3872959copy number variation1nstd102humanBenign GRCh37 chr2: 44,459,230-44,468,509 , GRCh38.p12 chr2: 44,232,091-44,241,370 PPM1B
    nsv3873702copy number variation1nstd102humanBenign GRCh37 chr2: 44,395,145-44,395,457 , GRCh38.p12 chr2: 44,168,006-44,168,318 PPM1B, PPM1B-DT
    nsv4451540copy number variation1nstd102humanPathogenic GRCh37 chr2: 44,438,045-44,546,016 , GRCh38.p12 chr2: 44,210,906-44,318,877 PPM1B, SLC3A1, 2 more genes
    nsv3874660copy number variation1nstd102humanUncertain significance GRCh37 chr2: 44,412,415-44,621,042 , GRCh38.p12 chr2: 44,185,276-44,393,903 PPM1B, RPL12P19, 3 more genes
    nsv3921838copy number variation1nstd102humanUncertain significance NCBI36 chr2: 44,319,444-44,400,041 , GRCh37.p13 chr2: 44,465,940-44,546,537 , GRCh38.p12 chr2: 44,238,801-44,319,398 PPM1B, PREPL, 2 more genes
    nsv3915129copy number variation1nstd102humanUncertain significance NCBI36 chr2: 44,301,241-44,457,105 , GRCh37.p13 chr2: 44,447,737-44,603,601 , GRCh38.p12 chr2: 44,220,598-44,376,462 PPM1B, CAMKMT, 3 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 PPM1B, CYP1B1-AS1, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 PPM1B, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 PPM1B, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 PPM1B, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 PPM1B, 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 PPM1B, 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 PPM1B, ALLC, 674 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 PPM1B, RPL7P13, 426 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 PPM1B, ATL2, 465 more genes
    nsv3882842copy number variation1nstd102humanPathogenic GRCh37 chr2: 34,792,916-56,676,541 , GRCh38.p12 chr2: 34,567,849-56,449,406 PPM1B, 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 PPM1B, RNU6-433P, 220 more genes
    nsv3919677inversion1nstd102humanPathogenic GRCh38.p12 chr2: 37,893,967-47,442,383 , GRCh37 chr2: 38,121,110-47,669,522 PPM1B, ASS1P2, 151 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 PPM1B, ACTG2, 1713 more genes
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