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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5980122insertion1nstd209human GRCh38 chr20: 59,881,322-59,881,322 , GRCh37.p13 chr20: 58,456,377-58,456,377 SYCP2
    nsv5971448insertion1nstd209human GRCh38 chr20: 59,872,533-59,872,533 , GRCh37.p13 chr20: 58,447,588-58,447,588 SYCP2
    nsv5872370copy number variation1nstd209human GRCh38 chr20: 59,904,991-59,906,390 , GRCh37.p13 chr20: 58,480,046-58,481,445 SYCP2
    nsv5526784copy number variation1nstd206human GRCh38 chr20: 59,897,624-59,900,338 , GRCh37.p13 chr20: 58,472,679-58,475,393 SYCP2
    nsv5519374copy number variation1nstd206human GRCh38 chr20: 59,879,313-59,879,367 , GRCh37.p13 chr20: 58,454,368-58,454,422 SYCP2
    nsv5350521translocation1nstd200human GRCh38 chr20: 59,868,212-59,868,212 , GRCh38 chr20: 59,868,360-59,868,360 , GRCh37.p13 chr20: 58,443,267-58,443,267 , GRCh37.p13 chr20: 58,443,415-58,443,415 SYCP2
    nsv5160888mobile element insertion1nstd203human GRCh38 chr20: 59,876,369-59,876,411 , GRCh37.p13 chr20: 58,451,424-58,451,466 SYCP2
    nsv5160468mobile element insertion1nstd203human GRCh38 chr20: 59,930,817-59,930,826 , GRCh37.p13 chr20: 58,505,872-58,505,881 SYCP2
    nsv5025770copy number variation1nstd200human GRCh38 chr20: 59,890,057-59,898,400 , GRCh37.p13 chr20: 58,465,112-58,473,455 SYCP2
    nsv5025769copy number variation1nstd200human GRCh38 chr20: 59,813,394-59,868,307 , GRCh37.p13 chr20: 58,388,449-58,443,362 SYCP2, RNU7-141P, 1 more genes
    nsv5022459copy number variation1nstd200human GRCh38 chr20: 59,928,987-59,929,061 , GRCh37.p13 chr20: 58,504,042-58,504,116 SYCP2
    nsv4854073copy number variation1nstd200human GRCh37 chr20: 58,506,645-58,507,005 , GRCh38.p12 chr20: 59,931,590-59,931,950 SYCP2, FAM217B
    nsv4854072copy number variation1nstd200human GRCh37 chr20: 58,504,042-58,504,116 , GRCh38.p12 chr20: 59,928,987-59,929,061 SYCP2
    nsv4727959copy number variation1nstd197human GRCh37 chr20: 58,443,469-58,456,547 , GRCh38.p12 chr20: 59,868,414-59,881,492 SYCP2
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4642906copy number variation2nstd186human GRCh37 chr20: 58,454,368-58,454,422 , GRCh38.p12 chr20: 59,879,313-59,879,367 SYCP2
    nsv4634022copy number variation1nstd183human GRCh37 chr20: 58,455,479-58,456,007 , GRCh38.p12 chr20: 59,880,424-59,880,952 SYCP2
    nsv4633484copy number variation1nstd183human GRCh37 chr20: 58,495,239-58,495,574 , GRCh38.p12 chr20: 59,920,184-59,920,519 SYCP2
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