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 185

    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
    nsv7069591inversion1nstd229human GRCh38 chr20: 105,288-375,237 , GRCh37.p13 chr20: 85,929-355,881 DEFB126, DEFB128, 9 more genes
    nsv7016287copy number variation1nstd229human GRCh38 chr20: 95,107-296,217 , GRCh37.p13 chr20: 75,748-276,858 DEFB129, ZCCHC3, 6 more genes
    nsv7015109copy number variation1nstd229human GRCh38 chr20: 212,701-479,100 , GRCh37.p13 chr20: 193,342-459,744 C20orf96, RBCK1, 10 more genes
    nsv7007834copy number variation1nstd229human GRCh38 chr20: 208,997-952,202 , GRCh37.p13 chr20: 189,638-932,845 TBC1D20, NRSN2-AS1, 19 more genes
    nsv6998549copy number variation1nstd229human GRCh38 chr20: 217,784-228,493 , GRCh37.p13 chr20: 198,425-209,134 DEFB129
    nsv6637884copy number variation1nstd102humanUncertain significance GRCh37 chr20: 79,455-347,319 , GRCh38.p12 chr20: 98,814-366,675 DEFB126, ZCCHC3, 9 more genes
    nsv6526289copy number variation1nstd223human GRCh38 chr20: 226,154-227,382 , GRCh37.p13 chr20: 206,795-208,023 DEFB129
    nsv6134047copy number variation1nstd213human GRCh37 chr20: 60,000-470,001 , GRCh38.p12 chr20: 79,361-489,357 RBCK1, DEFB126, 14 more genes
    nsv6133904copy number variation1nstd213human GRCh37 chr20: 1-1,970,001 , GRCh38.p12 chr20: 79,361-1,989,355 , CSNK2A1, 57 more genes
    nsv5934347copy number variation1nstd209human GRCh38 chr20: 206,512-250,903 , GRCh37.p13 chr20: 187,153-231,544 DEFB129
    nsv5884498copy number variation1nstd209human GRCh38 chr20: 226,163-228,596 , GRCh37.p13 chr20: 206,804-209,237 DEFB129
    nsv5868995copy number variation1nstd209human GRCh38 chr20: 207,922-237,184 , GRCh37.p13 chr20: 188,563-217,825 DEFB129
    nsv5558599inversion1nstd206human GRCh38 chr20: 213,086-231,936 , GRCh37.p13 chr20: 193,727-212,577 DEFB129
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5520553copy number variation1nstd206human GRCh38 chr20: 137,830-261,757 , GRCh37.p13 chr20: 118,471-242,398 DEFB126, DEFB127, 3 more genes
    nsv5381806copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198 DEFB132, LOC101929937, 24 more genes
    nsv5328186copy number variation1nstd204human GRCh38.p13 chr20: 226,131-227,411 , GRCh37.p13 chr20: 206,772-208,052 DEFB129
    nsv4861571copy number variation1nstd200human GRCh37 chr20: 206,795-208,023 , GRCh38.p12 chr20: 226,154-227,382 DEFB129
    nsv4729808copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,568-677,437 , GRCh38.p12 chr20: 80,927-696,793 CSNK2A1, SOX12, 18 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