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 299

    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
    nsv7095897copy number variation1nstd102humanUncertain significance GRCh37 chr20: 401,495-443,049 , GRCh38.p12 chr20: 420,851-462,405 TBC1D20, RBCK1
    nsv7077895inversion1nstd229human GRCh38 chr20: 265,739-1,834,868 , GRCh37.p13 chr20: 246,380-1,815,514 PSMF1, LOC105372498, 46 more genes
    nsv7016397copy number variation1nstd229human GRCh38 chr20: 455,532-459,879 , GRCh37.p13 chr20: 436,176-440,523 TBC1D20
    nsv7015417copy number variation1nstd229human GRCh38 chr20: 450,803-450,856 , GRCh37.p13 chr20: 431,447-431,500 TBC1D20
    nsv7015109copy number variation1nstd229human GRCh38 chr20: 212,701-479,100 , GRCh37.p13 chr20: 193,342-459,744 C20orf96, RBCK1, 10 more genes
    nsv7012737copy number variation1nstd229human GRCh38 chr20: 384,285-773,654 , GRCh37.p13 chr20: 364,929-754,298 SRXN1, RBCK1, 7 more genes
    nsv7007834copy number variation1nstd229human GRCh38 chr20: 208,997-952,202 , GRCh37.p13 chr20: 189,638-932,845 TBC1D20, NRSN2-AS1, 19 more genes
    nsv7000473copy number variation1nstd229human GRCh38 chr20: 449,155-453,193 , GRCh37.p13 chr20: 429,799-433,837 TBC1D20
    nsv6637610copy number variation1nstd102humanUncertain significance GRCh37 chr20: 384,444-744,450 , GRCh38.p12 chr20: 403,800-763,806 SCRT2, TBC1D20, 6 more genes
    nsv6637401copy number variation1nstd102humanUncertain significance GRCh37 chr20: 404,407-611,731 , GRCh38.p12 chr20: 423,763-631,087 TBC1D20, RBCK1, 2 more genes
    nsv6626688copy number variation1nstd224human GRCh37 chr20: 322,612-416,149 , GRCh38.p12 chr20: 341,968-435,505 RBCK1, TRIB3, 3 more genes
    nsv6626346copy number variation1nstd224human GRCh37 chr20: 372,097-484,926 , GRCh38.p12 chr20: 391,453-504,282 RBCK1, TBC1D20, 2 more genes
    nsv6626345copy number variation1nstd224human GRCh37 chr20: 368,739-512,067 , GRCh38.p12 chr20: 388,095-531,423 TBC1D20, RBCK1, 2 more genes
    nsv6599464inversion1nstd223human GRCh38 chr20: 448,444-449,098 , GRCh37.p13 chr20: 429,088-429,742 TBC1D20
    nsv6596619inversion1nstd223human GRCh38 chr20: 453,325-453,851 , GRCh37.p13 chr20: 433,969-434,495 TBC1D20
    nsv6596432inversion1nstd223human GRCh38 chr20: 455,681-456,826 , GRCh37.p13 chr20: 436,325-437,470 TBC1D20
    nsv6533657copy number variation1nstd223human GRCh38 chr20: 453,342-454,196 , GRCh37.p13 chr20: 433,986-434,840 TBC1D20
    nsv6524663copy number variation1nstd223human GRCh38 chr20: 418,542-506,050 , GRCh37.p13 chr20: 399,186-486,694 RBCK1, CSNK2A1, 1 more genes
    nsv6523547copy number variation1nstd223human GRCh38 chr20: 459,074-466,636 , GRCh37.p13 chr20: 439,718-447,280 TBC1D20
    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