U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 386

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916111copy number variation1nstd209human GRCh38 chr9: 5,543,514-5,543,574 , GRCh37.p13 chr9: 5,543,514-5,543,574 PDCD1LG2
    nsv5915802copy number variation1nstd209human GRCh38 chr9: 4,956,818-6,213,781 , GRCh37.p13 chr9: 4,956,818-6,213,781 , RLN1, 30 more genes
    nsv5910547copy number variation1nstd209human GRCh38 chr9: 5,516,627-5,516,780 , GRCh37.p13 chr9: 5,516,627-5,516,780 PDCD1LG2
    nsv5848981copy number variation1nstd209human GRCh38 chr9: 5,515,555-5,516,554 , GRCh37.p13 chr9: 5,515,555-5,516,554 PDCD1LG2
    nsv5713465mobile element insertion1nstd211human GRCh38 chr9: 5,509,964-5,509,964 , GRCh37.p13 chr9: 5,509,964-5,509,964 PDCD1LG2
    nsv5697449mobile element insertion2nstd211human GRCh38 chr9: 5,560,702-5,560,702 , GRCh37.p13 chr9: 5,560,702-5,560,702 PDCD1LG2
    nsv5635259insertion1nstd207human GRCh38 chr9: 5,560,685-5,560,685 , GRCh37.p13 chr9: 5,560,685-5,560,685 PDCD1LG2
    nsv5592398copy number variation1nstd207human GRCh38 chr9: 5,543,514-5,543,574 , GRCh37.p13 chr9: 5,543,514-5,543,574 PDCD1LG2
    nsv5489180copy number variation1nstd206human GRCh38 chr9: 5,525,124-5,525,863 , GRCh37.p13 chr9: 5,525,124-5,525,863 PDCD1LG2
    nsv5485413copy number variation1nstd206human GRCh38 chr9: 5,534,901-5,534,992 , GRCh37.p13 chr9: 5,534,901-5,534,992 PDCD1LG2
    nsv5484801copy number variation1nstd206human GRCh38 chr9: 5,516,631-5,516,781 , GRCh37.p13 chr9: 5,516,631-5,516,781 PDCD1LG2
    nsv5481917copy number variation1nstd206human GRCh38 chr9: 5,509,030-5,509,087 , GRCh37.p13 chr9: 5,509,030-5,509,087 PDCD1LG2
    nsv5474288copy number variation1nstd206human GRCh38 chr9: 5,543,515-5,543,575 , GRCh37.p13 chr9: 5,543,515-5,543,575 PDCD1LG2
    nsv5396072mobile element insertion1nstd206human GRCh38 chr9: 5,560,702-5,560,753 , GRCh37.p13 chr9: 5,560,702-5,560,753 PDCD1LG2
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5314214copy number variation1nstd204human GRCh38.p13 chr9: 4,872,969-5,692,972 , GRCh37.p13 chr9: 4,872,969-5,692,972 , INSL4, 23 more genes
    nsv5260071copy number variation1nstd204human GRCh38.p13 chr9: 5,564,208-5,565,451 , GRCh37.p13 chr9: 5,564,208-5,565,451 PDCD1LG2
    nsv5112630mobile element insertion1nstd203human GRCh38 chr9: 5,560,690-5,560,702 , GRCh37.p13 chr9: 5,560,690-5,560,702 PDCD1LG2
    nsv5108728mobile element insertion1nstd203human GRCh38 chr9: 5,560,688-5,560,702 , GRCh37.p13 chr9: 5,560,688-5,560,702 PDCD1LG2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center