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 472

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137757copy number variation1nstd102humanPathogenic GRCh38 chr7: 117,602,152-117,612,040 , GRCh37 chr7: 117,242,206-117,252,094 CFTR
    nsv6125593insertion1nstd186human GRCh37 chr7: 117,252,075-117,252,108 , GRCh38.p12 chr7: 117,612,021-117,612,054 CFTR
    nsv5926752copy number variation1nstd209human GRCh38 chr7: 117,626,743-117,626,983 , GRCh37.p13 chr7: 117,266,797-117,267,037 CFTR
    nsv5917776copy number variation1nstd209human GRCh38 chr7: 117,626,548-117,627,256 , GRCh37.p13 chr7: 117,266,602-117,267,310 CFTR
    nsv5915408copy number variation1nstd209human GRCh38 chr7: 117,647,117-117,647,319 , GRCh37.p13 chr7: 117,287,171-117,287,373 CFTR
    nsv5914268copy number variation1nstd209human GRCh38 chr7: 117,645,585-117,650,526 , GRCh37.p13 chr7: 117,285,639-117,290,580 CFTR
    nsv5852909copy number variation1nstd209human GRCh38 chr7: 117,552,281-117,555,196 , GRCh37.p13 chr7: 117,192,335-117,195,250 CFTR-AS1, CFTR
    nsv5728461mobile element insertion1nstd211human GRCh38 chr7: 117,606,482-117,606,482 , GRCh37.p13 chr7: 117,246,536-117,246,536 CFTR
    nsv5717142mobile element insertion1nstd211human GRCh38 chr7: 117,585,354-117,585,354 , GRCh37.p13 chr7: 117,225,408-117,225,408 CFTR
    nsv5686753mobile element insertion2nstd211human GRCh38 chr7: 117,645,848-117,645,848 , GRCh37.p13 chr7: 117,285,902-117,285,902 CFTR
    nsv5684129mobile element insertion2nstd211human GRCh38 chr7: 117,552,753-117,552,753 , GRCh37.p13 chr7: 117,192,807-117,192,807 CFTR, CFTR-AS1
    nsv5678298mobile element insertion1nstd211human GRCh38 chr7: 117,609,543-117,609,543 , GRCh37.p13 chr7: 117,249,597-117,249,597 CFTR
    nsv5674025copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,304,664-117,306,195 , GRCh38.p12 chr7: 117,664,610-117,666,141 CFTR
    nsv5674022copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,246,726-117,251,860 , GRCh38 chr7: 117,606,672-117,611,806 CFTR
    nsv5673932copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 117,267,556-117,267,869 , GRCh38.p12 chr7: 117,627,502-117,627,815 CFTR
    nsv5673930copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,218,381-117,254,777 , GRCh38.p12 chr7: 117,578,327-117,614,723 CFTR
    nsv5673929copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,174,320-117,176,752 , GRCh38.p12 chr7: 117,534,266-117,536,698 CFTR
    nsv5673928copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 117,170,943-117,171,255 , GRCh38.p12 chr7: 117,530,889-117,531,201 CFTR
    nsv5673842copy number variation1nstd102humanPathogenic GRCh37 chr7: 117,246,713-117,251,872 , GRCh38.p12 chr7: 117,606,659-117,611,818 CFTR
    nsv5673786copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 117,282,468-117,288,374 , GRCh38.p12 chr7: 117,642,414-117,648,320 CFTR
    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