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 436

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979848insertion1nstd209human GRCh38 chr19: 5,303,954-5,303,954 , GRCh37.p13 chr19: 5,303,965-5,303,965 PTPRS
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5969392insertion1nstd209human GRCh38 chr19: 5,233,977-5,233,977 , GRCh37.p13 chr19: 5,233,988-5,233,988 PTPRS
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5941391copy number variation1nstd209human GRCh38 chr19: 5,232,571-5,232,627 , GRCh37.p13 chr19: 5,232,582-5,232,638 PTPRS
    nsv5940898copy number variation1nstd209human GRCh38 chr19: 5,280,448-5,281,063 , GRCh37.p13 chr19: 5,280,459-5,281,074 PTPRS
    nsv5933306copy number variation1nstd209human GRCh38 chr19: 5,305,502-5,305,683 , GRCh37.p13 chr19: 5,305,513-5,305,694 PTPRS
    nsv5931496copy number variation1nstd209human GRCh38 chr19: 5,252,320-5,252,622 , GRCh37.p13 chr19: 5,252,331-5,252,633 PTPRS
    nsv5533981insertion1nstd206human GRCh38 chr19: 5,303,944-5,303,951 , GRCh37.p13 chr19: 5,303,955-5,303,962 PTPRS
    nsv5525534copy number variation1nstd206human GRCh38 chr19: 5,302,820-5,303,677 , GRCh37.p13 chr19: 5,302,831-5,303,688 PTPRS
    nsv5523928copy number variation1nstd206human GRCh38 chr19: 5,267,420-5,267,971 , GRCh37.p13 chr19: 5,267,431-5,267,982 PTPRS
    nsv5523840copy number variation1nstd206human GRCh38 chr19: 5,305,899-5,307,548 , GRCh37.p13 chr19: 5,305,910-5,307,559 PTPRS
    nsv5519570copy number variation1nstd206human GRCh38 chr19: 5,252,298-5,252,607 , GRCh37.p13 chr19: 5,252,309-5,252,618 PTPRS
    nsv5322876copy number variation1nstd204human GRCh37.p13 chr19: 5,292,393-5,298,154 , GRCh38.p13 chr19: 5,292,382-5,298,143 LOC105372253, PTPRS
    nsv5299997copy number variation1nstd204human GRCh38.p13 chr19: 5,292,347-5,298,221 , GRCh37.p13 chr19: 5,292,358-5,298,232 LOC105372253, PTPRS
    nsv5297445copy number variation1nstd204human GRCh38.p13 chr19: 5,264,601-5,269,900 , GRCh37.p13 chr19: 5,264,612-5,269,911 PTPRS
    nsv5291914copy number variation1nstd204human GRCh38.p13 chr19: 5,292,401-5,298,100 , GRCh37.p13 chr19: 5,292,412-5,298,111 PTPRS, LOC105372253
    nsv5175093mobile element insertion1nstd203human GRCh38 chr19: 5,253,282-5,253,282 , GRCh37.p13 chr19: 5,253,293-5,253,293 PTPRS
    nsv5163270mobile element insertion1nstd203human GRCh38 chr19: 5,242,428-5,242,476 , GRCh37.p13 chr19: 5,242,439-5,242,487 PTPRS
    nsv5027409copy number variation1nstd200human GRCh38 chr19: 5,309,906-5,311,193 , GRCh37.p13 chr19: 5,309,917-5,311,204 PTPRS
    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