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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096157copy number variation1nstd102humanPathogenic GRCh37 chr2: 3,391,395-3,428,454 , GRCh38.p12 chr2: 3,387,624-3,424,683 , GRCh38.p12 chr2|NT_187522.1: 1-34,747 TRAPPC12
    nsv4453222copy number variation1nstd102humanPathogenic GRCh37 chr2: 3,385,474-3,418,641 , GRCh38.p12 chr2|NT_187522.1: 1-22,973 , GRCh38.p12 chr2: 3,381,703-3,414,870 TRAPPC12
    nsv3904419copy number variation1nstd102humanLikely benign NCBI36 chr2: 3,271,089-3,392,949 , GRCh37 chr2: 3,292,082-3,413,942 , GRCh38 chr2: 3,288,311-3,410,171 TRAPPC12, EIPR1
    nsv4673940copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,202,277-3,397,677 , GRCh38.p12 chr2: 3,198,506-3,393,906 TRAPPC12, EIPR1
    nsv4450051copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,297,005-3,424,503 , GRCh38.p12 chr2: 3,293,234-3,420,732 TRAPPC12, EIPR1
    nsv6290666copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,281,275-3,394,543 , GRCh38.p12 chr2: 3,277,504-3,390,772 TRAPPC12, EIPR1
    nsv4674486copy number variation1nstd102humanLikely benign GRCh37 chr2: 3,001,017-3,494,850 , GRCh38.p12 chr2: 2,997,245-3,491,079 TRAPPC12, EIPR1, 3 more genes
    nsv6636911copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,293,810-3,488,006 , GRCh38.p12 chr2: 3,290,039-3,484,235 TRAPPC12, LOC112268321, 1 more genes
    nsv4674765copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,425,359-3,504,178 , GRCh38.p12 chr2: 3,421,588-3,500,407 , GRCh38.p12 chr2|NT_187522.1: 31,648-109,877 TRAPPC12, LOC112268321, 1 more genes
    nsv6290360copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,432,176-3,504,178 , GRCh38.p12 chr2: 3,428,405-3,500,407 , GRCh38.p12 chr2|NT_187522.1: 38,469-109,877 TRAPPC12, ADI1, 1 more genes
    nsv3899884copy number variation1nstd102humanPathogenic GRCh38 chr2: 30,341-3,449,132 , GRCh37 chr2: 30,341-3,452,903 , NCBI36 chr2: 20,341-3,431,910 TRAPPC12, EIPR1, 34 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 TRAPPC12, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 TRAPPC12, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 TRAPPC12, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 TRAPPC12, 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 TRAPPC12, 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 TRAPPC12, ALLC, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 TRAPPC12, 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 TRAPPC12, LOC105373394, 507 more genes
    nsv3907033copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531 TRAPPC12, GTF3C2-AS1, 434 more genes
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