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 417

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7076574inversion1nstd229human GRCh38 chr19: 3,237,321-3,237,348 , GRCh37.p13 chr19: 3,237,319-3,237,346 CELF5
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7065682inversion1nstd229human GRCh38 chr19: 3,282,406-3,593,791 , GRCh37.p13 chr19: 3,282,404-3,593,789 CELF5, NFIC, 11 more genes
    nsv7015264copy number variation1nstd229human GRCh38 chr19: 3,295,551-3,308,349 , GRCh37.p13 chr19: 3,295,549-3,308,347 LOC105372244, CELF5
    nsv7009174copy number variation1nstd229human GRCh38 chr19: 3,219,539-3,224,287 , GRCh37.p13 chr19: 3,219,537-3,224,285 CELF5
    nsv7008143copy number variation1nstd229human GRCh38 chr19: 3,255,101-3,308,100 , GRCh37.p13 chr19: 3,255,099-3,308,098 CELF5, LOC105372244
    nsv7004140copy number variation1nstd229human GRCh38 chr19: 3,270,522-3,270,565 , GRCh37.p13 chr19: 3,270,520-3,270,563 CELF5
    nsv7002827copy number variation1nstd229human GRCh38 chr19: 3,263,724-3,265,125 , GRCh37.p13 chr19: 3,263,722-3,265,123 CELF5
    nsv7001535copy number variation1nstd229human GRCh38 chr19: 3,260,417-3,269,323 , GRCh37.p13 chr19: 3,260,415-3,269,321 CELF5
    nsv6624862copy number variation1nstd224human GRCh37 chr19: 3,255,789-3,321,352 , GRCh38.p12 chr19: 3,255,791-3,321,354 CELF5, LOC105372244
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6534940copy number variation1nstd223human GRCh38 chr19: 3,241,130-3,241,844 , GRCh37.p13 chr19: 3,241,128-3,241,842 CELF5
    nsv6533945copy number variation1nstd223human GRCh38 chr19: 3,292,087-3,292,380 , GRCh37.p13 chr19: 3,292,085-3,292,378 CELF5
    nsv6532025copy number variation1nstd223human GRCh38 chr19: 3,265,878-3,268,147 , GRCh37.p13 chr19: 3,265,876-3,268,145 CELF5
    nsv6519590copy number variation1nstd223human GRCh38 chr19: 3,197,916-3,251,361 , GRCh37.p13 chr19: 3,197,914-3,251,359 CELF5, NCLN
    nsv6518781copy number variation1nstd223human GRCh38 chr19: 3,264,558-3,265,894 , GRCh37.p13 chr19: 3,264,556-3,265,892 CELF5
    nsv6242748mobile element insertion1nstd215human GRCh38 chr19: 3,264,316-3,264,316 , GRCh37.p13 chr19: 3,264,314-3,264,314 CELF5
    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