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 173

    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
    nsv7096019copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,063,276-3,218,325 , GRCh38.p12 chr20: 3,082,630-3,237,679 RN7SL555P, FASTKD5, 8 more genes
    nsv7095887copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,211,983-3,212,843 , GRCh38.p12 chr20: 3,231,337-3,232,197 SLC4A11
    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
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 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
    nsv7010860copy number variation1nstd229human GRCh38 chr20: 3,191,107-3,407,328 , GRCh37.p13 chr20: 3,171,753-3,387,975 ITPA, DNAAF9, 5 more genes
    nsv7001602copy number variation1nstd229human GRCh38 chr20: 3,193,194-3,244,957 , GRCh37.p13 chr20: 3,173,840-3,225,603 DDRGK1, ITPA, 1 more genes
    nsv6998610copy number variation1nstd229human GRCh38 chr20: 3,238,901-3,244,300 , GRCh37.p13 chr20: 3,219,547-3,224,946 SLC4A11
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6529546copy number variation1nstd223human GRCh38 chr20: 3,191,107-3,407,325 , GRCh37.p13 chr20: 3,171,753-3,387,972 DDRGK1, ITPA, 5 more genes
    nsv6524542copy number variation1nstd223human GRCh38 chr20: 3,234,264-3,262,127 , GRCh37.p13 chr20: 3,214,910-3,242,773 DNAAF9, SLC4A11
    nsv6516837copy number variation1nstd223human GRCh38 chr20: 3,238,885-3,244,296 , GRCh37.p13 chr20: 3,219,531-3,224,942 SLC4A11
    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
    nsv6223424copy number variation1nstd214human GRCh38 chr20: 3,228,032-3,228,085 , GRCh37.p13 chr20: 3,208,678-3,208,731 SLC4A11
    nsv6133803copy number variation1nstd213human GRCh37 chr20: 2,720,000-3,420,001 , GRCh38.p12 chr20: 2,739,354-3,439,354 AVP, GNRH2, 26 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