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 201

    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
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7010327copy number variation1nstd229human GRCh38 chr19: 3,179,744-3,180,073 , GRCh37.p13 chr19: 3,179,742-3,180,071 S1PR4
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6289699insertion1nstd214human GRCh38 chr19: 3,176,848-3,176,848 , GRCh37.p13 chr19: 3,176,846-3,176,846 S1PR4
    nsv6285165insertion1nstd214human GRCh38 chr19: 3,176,804-3,176,804 , GRCh37.p13 chr19: 3,176,802-3,176,802 S1PR4
    nsv6283958copy number variation1nstd214human GRCh38 chr19: 3,178,091-3,178,246 , GRCh37.p13 chr19: 3,178,089-3,178,244 S1PR4
    nsv6281696copy number variation1nstd214human GRCh38 chr19: 3,177,646-3,177,762 , GRCh37.p13 chr19: 3,177,644-3,177,760 S1PR4
    nsv6280816copy number variation1nstd214human GRCh38 chr19: 3,178,201-3,178,278 , GRCh37.p13 chr19: 3,178,199-3,178,276 S1PR4
    nsv6277977copy number variation1nstd214human GRCh38 chr19: 3,178,129-3,178,206 , GRCh37.p13 chr19: 3,178,127-3,178,204 S1PR4
    nsv6276790copy number variation1nstd214human GRCh38 chr19: 3,178,169-3,178,246 , GRCh37.p13 chr19: 3,178,167-3,178,244 S1PR4
    nsv6275934copy number variation1nstd214human GRCh38 chr19: 3,178,090-3,178,206 , GRCh37.p13 chr19: 3,178,088-3,178,204 S1PR4
    nsv6204070copy number variation1nstd214human GRCh38 chr19: 3,178,116-3,178,271 , GRCh37.p13 chr19: 3,178,114-3,178,269 S1PR4
    nsv6201435copy number variation1nstd214human GRCh38 chr19: 3,178,123-3,178,278 , GRCh37.p13 chr19: 3,178,121-3,178,276 S1PR4
    nsv6196477copy number variation1nstd214human GRCh38 chr19: 3,176,930-3,176,992 , GRCh37.p13 chr19: 3,176,928-3,176,990 S1PR4
    nsv6190508copy number variation1nstd214human GRCh38 chr19: 3,178,130-3,178,246 , GRCh37.p13 chr19: 3,178,128-3,178,244 S1PR4
    nsv6145940copy number variation1nstd206human GRCh38 chr19: 3,173,000-3,178,100 , GRCh37.p13 chr19: 3,172,998-3,178,098 S1PR4
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 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