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 177

    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
    nsv7071843inversion1nstd229human GRCh38 chr20: 62,912,832-62,944,154 , GRCh37.p13 chr20: 61,544,184-61,575,506 DIDO1, GID8
    nsv7064962inversion1nstd229human GRCh38 chr20: 62,710,955-62,963,614 , GRCh37.p13 chr20: 61,342,307-61,594,966 , GID8, 14 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
    nsv7021890copy number variation1nstd229human GRCh38 chr20: 62,944,201-62,963,600 , GRCh37.p13 chr20: 61,575,553-61,594,952 SLC17A9, GID8
    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
    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
    nsv6551088copy number variation1nstd223human GRCh38 chr20: 62,943,848-62,973,196 , GRCh37.p13 chr20: 61,575,200-61,604,548 GID8, SLC17A9
    nsv6540637copy number variation1nstd223human GRCh38 chr20: 62,937,201-62,938,800 , GRCh37.p13 chr20: 61,568,553-61,570,152 DIDO1, GID8
    nsv6538338copy number variation1nstd223human GRCh38 chr20: 62,908,105-62,940,494 , GRCh37.p13 chr20: 61,539,457-61,571,846 GID8, DIDO1
    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
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 HAR1A, PPDPF, 100 more genes
    nsv6311089copy number variation2nstd102humanUncertain significance GRCh37 chr20: 61,448,417-62,124,660 , GRCh38.p12 chr20: 62,817,065-63,493,307 ARFGAP1, LOC105376996, 33 more genes
    nsv6290337copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,038,552-62,907,579 , GRCh38.p12 chr20: 62,463,496-64,276,226 CHRNA4, COL9A3, 99 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