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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 TRMT61B, CYP1B1-AS1, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 TRMT61B, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 TRMT61B, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 TRMT61B, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 TRMT61B, 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 TRMT61B, 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 TRMT61B, ALLC, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 TRMT61B, LOC105374455, 504 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 TRMT61B, LOC105373394, 507 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 TRMT61B, RPL7P13, 426 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 TRMT61B, ATL2, 465 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 TRMT61B, GTF3C2-AS1, 316 more genes
    nsv3877469copy number variation1nstd102humanPathogenic GRCh37 chr2: 28,069,882-43,543,420 , GRCh38.p12 chr2: 27,847,015-43,316,281 TRMT61B, FOSL2, 219 more genes
    nsv3919769copy number variation1nstd102humanPathogenic NCBI36 chr2: 22,776,056-33,845,581 , GRCh37.p13 chr2: 22,922,551-33,992,077 , GRCh38.p12 chr2: 22,699,679-33,767,010 TRMT61B, RNA5SP88, 213 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 TRMT61B, ADCY3, 314 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 TRMT61B, LOC101927723, 1246 more genes
    nsv4454993copy number variation1nstd102humanUncertain significance GRCh37 chr2: 28,980,521-29,300,911 , GRCh38.p12 chr2: 28,757,655-29,078,045 TRMT61B, SNORD53B, 7 more genes
    nsv3901052copy number variation1nstd102humanUncertain significance NCBI36 chr2: 28,765,595-29,030,516 , GRCh38 chr2: 28,689,225-28,954,146 , GRCh37 chr2: 28,912,091-29,177,012 TRMT61B, PPP1CB, 7 more genes
    nsv4452277copy number variation1nstd102humanUncertain significance GRCh37 chr2: 29,030,646-29,289,738 , GRCh38.p12 chr2: 28,807,780-29,066,872 TRMT61B, PCARE, 6 more genes
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 TRMT61B, LOC105374381, 136 more genes
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