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 97

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv5901879copy number variation1nstd209human GRCh38 chr3: 129,976,332-129,976,433 , GRCh37.p13 chr3: 129,695,175-129,695,276 TRH
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4920090copy number variation1nstd200human GRCh38 chr3: 129,975,736-129,982,182 , GRCh37.p13 chr3: 129,694,579-129,701,025 TRH
    nsv4920089copy number variation1nstd200human GRCh38 chr3: 129,974,489-129,980,980 , GRCh37.p13 chr3: 129,693,332-129,699,823 TRH
    nsv4791028copy number variation1nstd200human GRCh37 chr3: 129,695,175-129,695,284 , GRCh38.p12 chr3: 129,976,332-129,976,441 TRH
    nsv4585126copy number variation1nstd183human GRCh37 chr3: 129,606,827-129,731,753 , GRCh38.p12 chr3: 129,887,984-130,012,910 TMCC1, TMCC1-DT, 2 more genes
    nsv4394901copy number variation1nstd174human GRCh37 chr3: 129,676,582-129,932,014 , GRCh38.p12 chr3: 129,957,739-130,213,171 , OR7E21P, 12 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 NPHP3-AS1, RNA5SP142, 218 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918088copy number variation1nstd102humanUncertain significance GRCh37 chr3: 129,574,527-130,255,023 , NCBI36 chr3: 131,057,217-131,737,713 , GRCh38 chr3: 129,855,684-130,536,179 TRH, OR7E129P, 17 more genes
    nsv3914757copy number variation1nstd102humanPathogenic NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997 CLSTN2-AS1, COPB2, 177 more genes
    nsv3912335copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 128,809,478-134,768,195 , GRCh37 chr3: 127,326,788-133,285,505 , GRCh38 chr3: 127,607,945-133,566,661 ACP3, FTH1P4, 130 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3883666copy number variation1nstd102humanUncertain significance GRCh37 chr3: 128,660,985-129,811,200 , GRCh38.p12 chr3: 128,942,142-130,092,357 RHO, GP9, 35 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