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 207

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7035588copy number variation1nstd229human GRCh38 chr20: 32,060,350-32,064,274 , GRCh37.p13 chr20: 30,648,153-30,652,077 HCK
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7020317copy number variation1nstd229human GRCh38 chr20: 32,093,097-32,096,107 , GRCh37.p13 chr20: 30,680,900-30,683,910 HCK
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6637514copy number variation1nstd102humanUncertain significance GRCh37 chr20: 30,299,729-30,687,587 , GRCh38.p12 chr20: 31,711,926-32,099,784 RNA5SP482, TTLL9, 13 more genes
    nsv6535102copy number variation1nstd223human GRCh38 chr20: 32,060,401-32,061,121 , GRCh37.p13 chr20: 30,648,204-30,648,924 HCK
    nsv6533629copy number variation1nstd223human GRCh38 chr20: 32,061,191-32,062,147 , GRCh37.p13 chr20: 30,648,994-30,649,950 HCK
    nsv6531620copy number variation1nstd223human GRCh38 chr20: 32,041,223-32,061,233 , GRCh37.p13 chr20: 30,629,026-30,649,036 HCK, RNA5SP482
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6134286copy number variation1nstd213human GRCh37 chr20: 30,610,000-30,990,001 , GRCh38.p12 chr20: 32,022,197-32,402,198 HCK, TM9SF4, 9 more genes
    nsv6133805copy number variation1nstd213human GRCh37 chr20: 30,440,000-30,730,001 , GRCh38.p12 chr20: 31,852,197-32,142,198 TTLL9, XKR7, 8 more genes
    nsv6059432copy number variation1nstd212human GRCh38 chr20: 32,046,912-32,050,490 , GRCh37.p13 chr20: 30,634,715-30,638,293 RNA5SP482, HCK
    nsv5954189copy number variation1nstd209human GRCh38 chr20: 32,061,191-32,062,146 , GRCh37.p13 chr20: 30,648,994-30,649,949 HCK
    nsv5540497insertion1nstd206human GRCh38 chr20: 32,061,233-32,061,233 , GRCh37.p13 chr20: 30,649,036-30,649,036 HCK
    nsv5532320copy number variation1nstd206human GRCh38 chr20: 32,061,142-32,062,094 , GRCh37.p13 chr20: 30,648,945-30,649,897 HCK
    nsv5518232copy number variation1nstd206human GRCh38 chr20: 32,061,000-32,066,100 , GRCh37.p13 chr20: 30,648,803-30,653,903 HCK
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    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