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 116

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 more genes
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7095551copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,063,276-3,903,941 , GRCh38.p12 chr20: 3,082,630-3,923,294 PANK2, MAVS, 31 more genes
    nsv7074742inversion1nstd229human GRCh38 chr20: 3,441,683-5,027,331 , GRCh37.p13 chr20: 3,422,330-5,007,977 MAVS, MIR103B2, 33 more genes
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7007840copy number variation1nstd229human GRCh38 chr20: 3,864,283-4,073,646 , GRCh37.p13 chr20: 3,844,930-4,054,293 RPL21P2, MAVS, 6 more genes
    nsv7006305copy number variation1nstd229human GRCh38 chr20: 3,792,209-4,972,873 , GRCh37.p13 chr20: 3,772,856-4,953,519 MIR103A2, LOC107985392, 23 more genes
    nsv6999763copy number variation1nstd229human GRCh38 chr20: 3,909,735-3,915,577 , GRCh37.p13 chr20: 3,890,382-3,896,224 PANK2, MIR103A2, 1 more genes
    nsv6626693copy number variation1nstd224human GRCh37 chr20: 3,896,337-4,137,918 , GRCh38.p12 chr20: 3,915,690-4,157,271 RNF24, SMOX, 5 more genes
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6315500copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,802,218-4,010,802 , GRCh38.p12 chr20: 2,821,572-4,030,155 DNAAF9, LOC105372508, 40 more genes
    nsv6289946copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,844,158-3,898,983 , GRCh38.p12 chr20: 3,863,511-3,918,336 PANK2, MIR103A2, 3 more genes
    nsv6133811copy number variation1nstd213human GRCh37 chr20: 3,830,000-4,480,001 , GRCh38.p12 chr20: 3,849,353-4,499,353 RNF24, SMOX, 9 more genes
    nsv6133808copy number variation1nstd213human GRCh37 chr20: 3,300,000-12,130,001 , GRCh38.p12 chr20: 3,319,353-12,149,353 BMP2, CDC25B, 126 more genes
    nsv5946328copy number variation1nstd209human GRCh38 chr20: 3,914,036-3,915,542 , GRCh37.p13 chr20: 3,894,683-3,896,189 PANK2, MIR103A2, 1 more genes
    nsv5934392copy number variation1nstd209human GRCh38 chr20: 3,792,203-4,972,872 , GRCh37.p13 chr20: 3,772,850-4,953,518 FTLP3, PANK2-AS1, 23 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