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 396

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    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
    nsv5941283copy number variation1nstd209human GRCh38 chr19: 3,861,366-3,861,664 , GRCh37.p13 chr19: 3,861,364-3,861,662 ZFR2
    nsv5939906copy number variation1nstd209human GRCh38 chr19: 3,830,915-3,830,992 , GRCh37.p13 chr19: 3,830,913-3,830,990 ZFR2
    nsv5936139copy number variation1nstd209human GRCh38 chr19: 3,837,408-3,837,531 , GRCh37.p13 chr19: 3,837,406-3,837,529 ZFR2
    nsv5929375copy number variation1nstd209human GRCh38 chr19: 3,866,388-3,866,448 , GRCh37.p13 chr19: 3,866,386-3,866,446 ZFR2
    nsv5884743copy number variation1nstd209human GRCh38 chr19: 3,816,161-3,817,360 , GRCh37.p13 chr19: 3,816,159-3,817,358 ZFR2
    nsv5645109insertion2nstd207human GRCh38 chr19: 3,820,818-3,820,818 , GRCh37.p13 chr19: 3,820,816-3,820,816 ZFR2
    nsv5602177copy number variation1nstd207human GRCh38 chr19: 3,820,807-3,820,914 , GRCh37.p13 chr19: 3,820,805-3,820,912 ZFR2
    nsv5586971copy number variation1nstd207human GRCh38 chr19: 3,808,037-3,808,118 , GRCh37.p13 chr19: 3,808,035-3,808,116 ZFR2
    nsv5586623copy number variation1nstd207human GRCh38 chr19: 3,816,345-3,817,748 , GRCh37.p13 chr19: 3,816,343-3,817,746 ZFR2
    nsv5586317copy number variation1nstd207human GRCh38 chr19: 3,866,388-3,866,448 , GRCh37.p13 chr19: 3,866,386-3,866,446 ZFR2
    nsv5562938sequence alteration1nstd206human GRCh38 chr19: 3,816,533-3,826,930 , GRCh37.p13 chr19: 3,816,531-3,826,928 ZFR2
    nsv5532318copy number variation1nstd206human GRCh38 chr19: 3,800,519-3,847,305 , GRCh37.p13 chr19: 3,800,517-3,847,303 ZFR2, MATK
    nsv5532232copy number variation1nstd206human GRCh38 chr19: 3,826,336-3,826,466 , GRCh37.p13 chr19: 3,826,334-3,826,464 ZFR2
    nsv5528119copy number variation1nstd206human GRCh38 chr19: 3,833,025-3,839,350 , GRCh37.p13 chr19: 3,833,023-3,839,348 ZFR2
    nsv5526007copy number variation1nstd206human GRCh38 chr19: 3,816,348-3,817,749 , GRCh37.p13 chr19: 3,816,346-3,817,747 ZFR2
    nsv5525588copy number variation1nstd206human GRCh38 chr19: 3,824,592-3,828,588 , GRCh37.p13 chr19: 3,824,590-3,828,586 ZFR2
    nsv5515795copy number variation1nstd206human GRCh38 chr19: 3,816,465-3,826,795 , GRCh37.p13 chr19: 3,816,463-3,826,793 ZFR2
    nsv5381271copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,762,699-3,808,981 , GRCh38.p12 chr19: 3,762,701-3,808,983 MATK, RAX2, 3 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