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 250

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950698insertion1nstd209human GRCh38 chr3: 119,738,332-119,738,332 , GRCh37.p13 chr3: 119,457,179-119,457,179 CFAP91
    nsv5901427copy number variation1nstd209human GRCh38 chr3: 119,722,771-119,722,845 , GRCh37.p13 chr3: 119,441,618-119,441,692 CFAP91
    nsv5900343copy number variation1nstd209human GRCh38 chr3: 119,701,066-119,701,493 , GRCh37.p13 chr3: 119,419,913-119,420,340 LOC105374064, CFAP91
    nsv5889494copy number variation1nstd209human GRCh38 chr3: 119,662,960-119,757,421 , GRCh37.p13 chr3: 119,381,807-119,476,268 LOC105374064, CFAP91, 2 more genes
    nsv5834860copy number variation1nstd209human GRCh38 chr3: 119,708,165-119,756,578 , GRCh37.p13 chr3: 119,427,012-119,475,425 CFAP91
    nsv5690527mobile element insertion1nstd211human GRCh38 chr3: 119,702,343-119,702,343 , GRCh37.p13 chr3: 119,421,190-119,421,190 LOC105374064, CFAP91
    nsv5688426mobile element insertion1nstd211human GRCh38 chr3: 119,753,424-119,753,424 , GRCh37.p13 chr3: 119,472,271-119,472,271 CFAP91
    nsv5684998mobile element insertion2nstd211human GRCh38 chr3: 119,750,532-119,750,532 , GRCh37.p13 chr3: 119,469,379-119,469,379 CFAP91
    nsv5678618mobile element insertion1nstd211human GRCh38 chr3: 119,717,569-119,717,569 , GRCh37.p13 chr3: 119,436,416-119,436,416 CFAP91
    nsv5674768mobile element insertion1nstd211human GRCh38 chr3: 119,731,324-119,731,324 , GRCh37.p13 chr3: 119,450,171-119,450,171 CFAP91
    nsv5577400copy number variation1nstd207human GRCh38 chr3: 119,701,066-119,701,493 , GRCh37.p13 chr3: 119,419,913-119,420,340 CFAP91, LOC105374064
    nsv5450371copy number variation1nstd206human GRCh38 chr3: 119,713,592-119,713,903 , GRCh37.p13 chr3: 119,432,439-119,432,750 CFAP91
    nsv5440478copy number variation1nstd206human GRCh38 chr3: 119,722,771-119,722,846 , GRCh37.p13 chr3: 119,441,618-119,441,693 CFAP91
    nsv5438716copy number variation1nstd206human GRCh38 chr3: 119,701,072-119,701,496 , GRCh37.p13 chr3: 119,419,919-119,420,343 LOC105374064, CFAP91
    nsv5401702mobile element insertion1nstd206human GRCh38 chr3: 119,750,532-119,750,583 , GRCh37.p13 chr3: 119,469,379-119,469,430 CFAP91
    nsv5394441mobile element insertion1nstd206human GRCh38 chr3: 119,753,424-119,753,475 , GRCh37.p13 chr3: 119,472,271-119,472,322 CFAP91
    nsv5346461translocation1nstd200human GRCh38 chr3: 119,722,771-119,722,771 , GRCh38 chr3: 119,722,846-119,722,846 , GRCh37.p13 chr3: 119,441,618-119,441,618 , GRCh37.p13 chr3: 119,441,693-119,441,693 CFAP91
    nsv5317048copy number variation1nstd204human GRCh37.p13 chr3: 119,416,898-119,426,875 , GRCh38.p13 chr3: 119,698,051-119,708,028 CFAP91, LOC105374064
    nsv5306786copy number variation1nstd204human GRCh37.p13 chr3: 119,419,919-119,420,343 , GRCh38.p13 chr3: 119,701,072-119,701,496 CFAP91, LOC105374064
    nsv5238510copy number variation1nstd204human GRCh38.p13 chr3: 119,757,801-119,762,300 , GRCh37.p13 chr3: 119,476,648-119,481,147 CFAP91
    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