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 371

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148072copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 193,343,827-194,599,635 , GRCh38.p12 chr3: 193,626,038-194,878,906 CPN2, GP5, 36 more genes
    nsv7144719copy number variation1nstd232human GRCh37.p13 chr3: 193,361,233-193,361,315 , GRCh38.p12 chr3: 193,643,444-193,643,526 OPA1
    nsv7144473insertion1nstd232human GRCh37.p13 chr3: 193,361,416-193,361,416 , GRCh38.p12 chr3: 193,643,627-193,643,627 OPA1
    nsv7096707copy number variation1nstd102humanPathogenic GRCh37 chr3: 193,360,534-193,361,914 , GRCh38.p12 chr3: 193,642,745-193,644,125 OPA1
    nsv7096706copy number variation1nstd102humanPathogenic GRCh37 chr3: 193,354,964-193,355,090 , GRCh38.p12 chr3: 193,637,175-193,637,301 OPA1
    nsv7096560copy number variation1nstd102humanPathogenic GRCh37 chr3: 193,382,649-193,384,198 , GRCh38.p12 chr3: 193,664,860-193,666,409 LOC102724808, OPA1
    nsv7096559copy number variation1nstd102humanPathogenic GRCh37 chr3: 193,332,492-193,336,745 , GRCh38.p12 chr3: 193,614,703-193,618,956 OPA1-AS1, OPA1
    nsv7096558copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,207,380-193,385,089 , GRCh38.p12 chr3: 193,489,591-193,667,300 ATP13A4-AS1, ATP13A4, 4 more genes
    nsv7096455copy number variation1nstd102humanPathogenic GRCh37 chr3: 193,380,591-193,385,089 , GRCh38.p12 chr3: 193,662,802-193,667,300 OPA1, LOC102724808
    nsv7093273copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr3: 193,384,968-193,385,074 , GRCh38 chr3: 193,667,179-193,667,285 OPA1, LOC102724808
    nsv7048883inversion1nstd229human GRCh38 chr3: 193,672,936-193,683,176 , GRCh37.p13 chr3: 193,390,725-193,400,965 OPA1, LOC102724808
    nsv6731794copy number variation1nstd229human GRCh38 chr3: 193,606,301-193,699,100 , GRCh37.p13 chr3: 193,324,090-193,416,889 LOC102724808, OPA1-AS1, 1 more genes
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6730584copy number variation1nstd229human GRCh38 chr3: 193,598,619-193,598,817 , GRCh37.p13 chr3: 193,316,408-193,316,606 OPA1
    nsv6722091copy number variation1nstd229human GRCh38 chr3: 193,686,114-193,686,518 , GRCh37.p13 chr3: 193,403,903-193,404,307 OPA1
    nsv6636634copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,396,762-195,009,038 , GRCh38.p12 chr3: 193,678,973-195,288,309 LINC02036, LINC02026, 45 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6313527copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,607,378-194,745,252 , GRCh38.p12 chr3: 192,889,589-195,024,523 LINC02036, HES1, 48 more genes
    nsv6311978copy number variation1nstd102humanPathogenic GRCh37 chr3: 193,382,649-193,385,089 , GRCh38.p12 chr3: 193,664,860-193,667,300 OPA1, LOC102724808
    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