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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944073copy number variation1nstd209human GRCh38 chr19: 42,242,322-42,266,502 , GRCh37.p13 chr19: 42,746,474-42,770,654 ERF, GSK3A
    nsv5884317copy number variation1nstd209human GRCh38 chr19: 42,242,378-42,253,700 , GRCh37.p13 chr19: 42,746,530-42,757,852 GSK3A, ERF
    nsv5564524copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,198,610-42,249,880 , GRCh37.p13 chr19: 42,702,762-42,754,032 ERF, ZNF526, 2 more genes
    nsv5564519copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,987,984-42,252,574 , GRCh37.p13 chr19: 42,514,712-42,756,726 GRIK5, DEDD2, 8 more genes
    nsv5564317copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,983,952-42,247,520 , GRCh37.p13 chr19: 42,514,712-42,751,672 GSK3A, ZNF574, 8 more genes
    nsv5564234copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,227,530-42,259,211 , GRCh37.p13 chr19: 42,731,682-42,763,363 GSK3A, ERF, 1 more genes
    nsv5564233copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,032,860-42,297,536 , GRCh37.p13 chr19: 42,537,012-42,801,688 POU2F2, ERF, 9 more genes
    nsv5564232copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,952,441-42,266,625 , GRCh37.p13 chr19: 42,514,712-42,770,777 CIC, ERF, 10 more genes
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5523303copy number variation1nstd206human GRCh38 chr19: 42,243,126-42,243,201 , GRCh37.p13 chr19: 42,747,278-42,747,353 GSK3A
    nsv5020520copy number variation1nstd200human GRCh38 chr19: 42,243,126-42,243,201 , GRCh37.p13 chr19: 42,747,278-42,747,353 GSK3A
    nsv5020519copy number variation1nstd200human GRCh38 chr19: 42,233,410-42,233,471 , GRCh37.p13 chr19: 42,737,562-42,737,623 GSK3A
    nsv4727924copy number variation1nstd197human GRCh38.p12 chr19: 42,234,354-42,234,678 , GRCh37 chr19: 42,738,506-42,738,830 GSK3A
    nsv4501893mobile element insertion1nstd166human GRCh37.p13 chr19: 42,747,169-42,747,169 , GRCh38.p12 chr19: 42,243,017-42,243,017 GSK3A
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4271680copy number variation1nstd166human GRCh37.p13 chr19: 42,737,562-42,737,623 , GRCh38.p12 chr19: 42,233,410-42,233,471 GSK3A
    nsv3921916copy number variation1nstd102humanPathogenic NCBI36 chr19: 47,126,886-48,337,448 , GRCh37 chr19: 42,514,712-43,645,608 , GRCh38 chr19: 41,930,894-43,141,456 PSG6, RABAC1, 42 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 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