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 300

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958185insertion1nstd209human GRCh38 chr6: 36,768,225-36,768,225 , GRCh37.p13 chr6: 36,736,002-36,736,002 CPNE5
    nsv5948576insertion1nstd209human GRCh38 chr6: 36,834,278-36,834,278 , GRCh37.p13 chr6: 36,802,054-36,802,054 CPNE5, C6orf89
    nsv5903284copy number variation1nstd209human GRCh38 chr6: 36,767,182-36,770,867 , GRCh37.p13 chr6: 36,734,959-36,738,644 CPNE5
    nsv5845589copy number variation1nstd209human GRCh38 chr6: 36,767,171-36,770,872 , GRCh37.p13 chr6: 36,734,948-36,738,649 CPNE5
    nsv5729312mobile element insertion1nstd211human GRCh38 chr6: 36,809,771-36,809,771 , GRCh37.p13 chr6: 36,777,547-36,777,547 CPNE5
    nsv5684956mobile element insertion1nstd211human GRCh38 chr6: 36,829,869-36,829,869 , GRCh37.p13 chr6: 36,797,645-36,797,645 CPNE5
    nsv5680518mobile element insertion1nstd211human GRCh38 chr6: 36,782,994-36,782,994 , GRCh37.p13 chr6: 36,750,771-36,750,771 CPNE5
    nsv5460898copy number variation1nstd206human GRCh38 chr6: 36,802,002-36,802,775 , GRCh37.p13 chr6: 36,769,778-36,770,551 CPNE5
    nsv5396663mobile element insertion1nstd206human GRCh38 chr6: 36,782,994-36,783,045 , GRCh37.p13 chr6: 36,750,771-36,750,822 CPNE5
    nsv5362858translocation1nstd200human GRCh38 chr6: 36,762,058-36,762,058 , GRCh38 chr6: 36,762,135-36,762,135 , GRCh37.p13 chr6: 36,729,912-36,729,912 , GRCh37.p13 chr6: 36,729,835-36,729,835 CPNE5
    nsv5331026translocation1nstd200human GRCh37 chr6: 36,729,835-36,729,835 , GRCh37 chr6: 36,729,912-36,729,912 , GRCh38.p12 chr6: 36,762,058-36,762,058 , GRCh38.p12 chr6: 36,762,135-36,762,135 CPNE5
    nsv5317518copy number variation1nstd204human GRCh37.p13 chr6: 36,802,532-36,803,762 , GRCh38.p13 chr6: 36,834,756-36,835,986 CPNE5, C6orf89
    nsv5309894copy number variation1nstd204human GRCh37.p13 chr6: 36,798,984-36,803,252 , GRCh38.p13 chr6: 36,831,208-36,835,476 CPNE5, C6orf89
    nsv5236832copy number variation1nstd204human GRCh38.p13 chr6: 36,831,552-36,835,633 , GRCh37.p13 chr6: 36,799,328-36,803,409 CPNE5, C6orf89
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5109824mobile element insertion1nstd203human GRCh38 chr6: 36,799,466-36,799,480 , GRCh37.p13 chr6: 36,767,243-36,767,257 CPNE5
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4940923copy number variation1nstd200human GRCh38 chr6: 36,836,650-36,837,548 , GRCh37.p13 chr6: 36,804,426-36,805,324 CPNE5, C6orf89
    nsv4940922copy number variation1nstd200human GRCh38 chr6: 36,831,214-36,835,473 , GRCh37.p13 chr6: 36,798,990-36,803,249 CPNE5, C6orf89
    nsv4940921copy number variation1nstd200human GRCh38 chr6: 36,825,205-36,825,341 , GRCh37.p13 chr6: 36,792,981-36,793,117 CPNE5
    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