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 123

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5552788insertion1nstd206human GRCh38 chr20: 57,391,962-57,392,006 , GRCh37.p13 chr20: 55,967,018-55,967,062 RBM38-AS1, RBM38
    nsv5532550copy number variation1nstd206human GRCh38 chr20: 57,392,778-57,393,227 , GRCh37.p13 chr20: 55,967,834-55,968,283 RBM38, RBM38-AS1
    nsv5518214copy number variation1nstd206human GRCh38 chr20: 57,391,820-57,392,653 , GRCh37.p13 chr20: 55,966,876-55,967,709 RBM38-AS1, RBM38
    nsv5160568mobile element insertion1nstd203human GRCh38 chr20: 57,383,966-57,383,978 , GRCh37.p13 chr20: 55,959,022-55,959,034 RBM38-AS1
    nsv5013333copy number variation1nstd200human GRCh38 chr20: 57,381,467-57,384,860 , GRCh37.p13 chr20: 55,956,523-55,959,916 RBM38-AS1
    nsv4854018copy number variation1nstd200human GRCh37 chr20: 55,956,523-55,959,916 , GRCh38.p12 chr20: 57,381,467-57,384,860 RBM38-AS1
    nsv4678958copy number variation1nstd189human GRCh37.p13 chr20: 55,665,635-56,143,223 , GRCh38.p12 chr20: 57,090,579-57,568,167 BMP7, PCK1, 17 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4625291copy number variation1nstd183human GRCh37 chr20: 55,816,772-56,085,952 , GRCh38.p12 chr20: 57,241,716-57,510,896 BMP7, RBM38-AS1, 13 more genes
    nsv4512407mobile element insertion1nstd166human GRCh37.p13 chr20: 55,959,022-55,959,022 , GRCh38.p12 chr20: 57,383,966-57,383,966 RBM38-AS1
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4285569copy number variation1nstd166human GRCh37.p13 chr20: 55,956,523-55,959,916 , GRCh38.p12 chr20: 57,381,467-57,384,860 RBM38-AS1
    nsv4284156copy number variation1nstd166human GRCh37.p13 chr20: 55,950,000-55,959,000 , GRCh38.p12 chr20: 57,374,944-57,383,944 RAE1, RBM38-AS1
    nsv4275037copy number variation1nstd166human GRCh37.p13 chr20: 55,859,838-56,531,739 , GRCh38.p12 chr20: 57,284,782-57,956,683 , MTND1P9, 17 more genes
    nsv3961531copy number variation1nstd168human GRCh38 chr20: 57,375,314-57,400,215 , GRCh37.p13 chr20: 55,950,370-55,975,271 RAE1, RBM38, 1 more genes
    nsv3920603copy number variation1nstd102humanUncertain significance NCBI36 chr20: 54,937,617-55,430,904 , GRCh38 chr20: 56,929,154-57,422,442 , GRCh37 chr20: 55,504,210-55,997,498 RPL39P39, LOC105372686, 14 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918295copy number variation1nstd102humanPathogenic GRCh38 chr20: 54,594,888-58,190,583 , NCBI36 chr20: 52,644,834-56,199,045 , GRCh37 chr20: 53,211,427-56,765,639 MTRNR2L3, LOC105372687, 59 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 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