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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885883copy number variation1nstd102humanLikely benign GRCh37 chr2: 31,435,578-31,661,595 , GRCh38.p12 chr2: 31,212,712-31,438,729 CAPN14, XDH, 3 more genes
    nsv3920389copy number variation1nstd102humanUncertain significance NCBI36 chr2: 31,285,190-31,517,788 , GRCh37.p13 chr2: 31,431,686-31,664,284 , GRCh38.p12 chr2: 31,208,820-31,441,418 CAPN14, EHD3, 3 more genes
    nsv6290466copy number variation1nstd102humanUncertain significance GRCh37 chr2: 31,431,801-31,661,595 , GRCh38.p12 chr2: 31,208,935-31,438,729 CAPN14, RNA5SP90, 3 more genes
    nsv4452726copy number variation2nstd102humanUncertain significance GRCh37 chr2: 31,434,360-31,658,788 , GRCh38.p12 chr2: 31,211,494-31,435,922 CAPN14, RNA5SP90, 3 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CAPN14, 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 CAPN14, LOC107985870, 161 more genes
    nsv4454991copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,940,473-36,813,297 , GRCh38.p12 chr2: 29,717,607-36,586,154 CAPN14, LOC105374435, 71 more genes
    nsv3885614copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,240,004-32,380,876 , GRCh38.p12 chr2: 29,017,138-32,155,807 CAPN14, LOC107985861, 32 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 CAPN14, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 CAPN14, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 CAPN14, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 CAPN14, 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 CAPN14, 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 CAPN14, ALLC, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 CAPN14, 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 CAPN14, LOC105373394, 507 more genes
    nsv3875055copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850 CAPN14, RPL7P13, 426 more genes
    nsv3879320copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230 CAPN14, ATL2, 465 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 CAPN14, 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 CAPN14, FOSL2, 219 more genes
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