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 167

    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
    nsv7095905copy number variation1nstd102humanUncertain significance GRCh37 chr20: 5,086,814-5,295,015 , GRCh38.p12 chr20: 5,106,168-5,314,369 UBE2D3P1, PCNA-AS1, 4 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
    nsv7074668inversion1nstd229human GRCh38 chr20: 5,297,411-5,297,440 , GRCh37.p13 chr20: 5,278,057-5,278,086 PROKR2
    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
    nsv7015435copy number variation1nstd229human GRCh38 chr20: 4,445,183-5,667,683 , GRCh37.p13 chr20: 4,425,830-5,648,329 LOC107985411, LOC105372510, 26 more genes
    nsv7008977copy number variation1nstd229human GRCh38 chr20: 4,351,306-5,587,282 , GRCh37.p13 chr20: 4,331,953-5,567,928 LINC00658, GPCPD1, 26 more genes
    nsv7007847copy number variation1nstd229human GRCh38 chr20: 5,051,802-5,318,241 , GRCh37.p13 chr20: 5,032,448-5,298,887 UBE2D3P1, PROKR2, 5 more genes
    nsv7006167copy number variation1nstd229human GRCh38 chr20: 5,301,776-5,305,756 , GRCh37.p13 chr20: 5,282,422-5,286,402 PROKR2
    nsv7000856copy number variation1nstd229human GRCh38 chr20: 5,289,333-5,306,368 , GRCh37.p13 chr20: 5,269,979-5,287,014 PROKR2, UBE2D3P1
    nsv6626789copy number variation1nstd224human GRCh37 chr20: 5,260,540-5,397,328 , GRCh38.p12 chr20: 5,279,894-5,416,682 PROKR2, UBE2D3P1, 1 more genes
    nsv6626788copy number variation1nstd224human GRCh37 chr20: 5,204,639-8,101,337 , GRCh38.p12 chr20: 5,223,993-8,120,690 BMP2, EIF4EP1, 39 more genes
    nsv6523321copy number variation1nstd223human GRCh38 chr20: 5,299,913-5,312,306 , GRCh37.p13 chr20: 5,280,559-5,292,952 PROKR2
    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
    nsv6291700copy number variation1nstd102humanUncertain significance GRCh37 chr20: 5,291,150-5,923,746 , GRCh38.p12 chr20: 5,310,504-5,943,100 CHGB, PROKR2, 14 more genes
    nsv6134039copy number variation1nstd213human GRCh37 chr20: 4,990,000-5,290,001 , GRCh38.p12 chr20: 5,009,354-5,309,355 PCNA, CDS2, 7 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
    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