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 155

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7095910copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857 LINC01749, HAR1A, 32 more genes
    nsv7075234inversion1nstd229human GRCh38 chr20: 62,886,537-63,022,704 , GRCh37.p13 chr20: 61,517,889-61,654,056 LINC01749, GID8, 3 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7037073copy number variation1nstd229human GRCh38 chr20: 62,978,683-63,027,504 , GRCh37.p13 chr20: 61,610,035-61,658,856 LINC01749, BHLHE23, 1 more genes
    nsv7035502copy number variation1nstd229human GRCh38 chr20: 62,999,313-63,140,948 , GRCh37.p13 chr20: 61,630,665-61,772,300 BHLHE23, HAR1B, 7 more genes
    nsv7033621copy number variation1nstd229human GRCh38 chr20: 62,954,078-63,070,134 , GRCh37.p13 chr20: 61,585,430-61,701,486 LINC01056, BHLHE23, 4 more genes
    nsv7032191copy number variation1nstd229human GRCh38 chr20: 63,004,701-63,032,900 , GRCh37.p13 chr20: 61,636,053-61,664,252 LINC00029, LINC01749, 2 more genes
    nsv7030059copy number variation1nstd229human GRCh38 chr20: 62,991,335-63,050,687 , GRCh37.p13 chr20: 61,622,687-61,682,039 LINC00029, LINC01749, 3 more genes
    nsv7021453copy number variation1nstd229human GRCh38 chr20: 62,945,997-63,054,654 , GRCh37.p13 chr20: 61,577,349-61,686,006 GID8, SLC17A9, 5 more genes
    nsv7021164copy number variation1nstd229human GRCh38 chr20: 62,972,878-63,016,807 , GRCh37.p13 chr20: 61,604,230-61,648,159 LINC01749, BHLHE23
    nsv7018842copy number variation1nstd229human GRCh38 chr20: 62,995,087-63,118,851 , GRCh37.p13 chr20: 61,626,439-61,750,203 HAR1A, LINC01749, 6 more genes
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6626831copy number variation1nstd224human GRCh37 chr20: 61,588,202-61,793,778 , GRCh38.p12 chr20: 62,956,850-63,162,426 LOC105376996, LINC01749, 8 more genes
    nsv6553327copy number variation1nstd223human GRCh38 chr20: 63,004,755-63,032,849 , GRCh37.p13 chr20: 61,636,107-61,664,201 LOC105372718, LINC01749, 2 more genes
    nsv6549808copy number variation1nstd223human GRCh38 chr20: 62,999,700-63,008,454 , GRCh37.p13 chr20: 61,631,052-61,639,806 BHLHE23, LINC01749
    nsv6315308copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,800,345-63,644,611 , GRCh37.p13 chr20: 60,375,401-62,275,964 STMN3, RPS21, 86 more genes
    nsv6315031copy number variation1nstd102humanUncertain significance GRCh38 chr20: 62,941,782-63,658,260 , GRCh37.p13 chr20: 61,573,134-62,289,613 GMEB2, LOC105372724, 38 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