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 67

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4674450copy number variation1nstd102humanUncertain significance GRCh37 chr3: 89,369,130-90,485,949 , GRCh38.p12 chr3: 89,319,980-90,436,799 MTCO2P6, PROS2P, 6 more genes
    nsv4568251inversion1nstd166human GRCh37.p13 chr3: 81,845,861-90,137,796 , GRCh38.p12 chr3: 81,796,710-90,088,646 POU1F1, CHMP2B, 54 more genes
    nsv4373112copy number variation1nstd173human GRCh37 chr3: 89,439,115-89,639,259 , GRCh38.p12 chr3: 89,389,965-89,590,109 MTATP6P6, EPHA3, 3 more genes
    nsv3923231copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 76,896,101-89,814,775 , GRCh37 chr3: 76,813,411-89,732,085 , GRCh38 chr3: 76,764,260-89,682,935 EPHA3, GBE1, 80 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3912034copy number variation1nstd102humanPathogenic GRCh38 chr3: 82,912,987-90,179,222 , GRCh37 chr3: 82,962,138-90,228,372 , NCBI36 chr3: 83,044,828-90,311,062 MTATP6P6, SNORA95, 49 more genes
    nsv3911768copy number variation1nstd102humanPathogenic NCBI36 chr3: 73,956,712-90,585,539 , GRCh37 chr3: 73,874,022-90,502,849 , GRCh38 chr3: 73,824,871-90,453,699 RN7SKP284, OR7E121P, 122 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
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3876149copy number variation1nstd102humanBenign GRCh37 chr3: 89,417,287-89,686,064 , GRCh38.p12 chr3: 89,368,137-89,636,914 MTATP6P6, MTCO2P6, 3 more genes
    nsv3874413copy number variation1nstd102humanBenign GRCh37 chr3: 89,440,509-90,504,539 , GRCh38.p12 chr3: 89,391,359-90,455,389 HSPE1P19, MTCO3P6, 6 more genes
    nsv2786695copy number variation2nstd132human NCBI36 chr3: 89,485,137-89,742,812 , GRCh37.p13 chr3: 89,402,447-89,660,122 , GRCh38.p12 chr3: 89,353,297-89,610,972 MTCO1P6, MTCO2P6, 3 more genes
    nsv2783692copy number variation1nstd132human NCBI36 chr3: 89,485,137-89,849,080 , GRCh37.p13 chr3: 89,402,447-89,766,390 , GRCh38.p12 chr3: 89,353,297-89,717,240 MTCO3P6, EPHA3, 3 more genes
    esv3831176copy number variation1estd219human GRCh37 chr3: 89,539,815-89,797,083 , GRCh38.p12 chr3: 89,490,665-89,747,933 MTCO1P6, MTCO2P6, 2 more genes
    nsv2757358copy number variation1nstd130human GRCh37 chr3: 89,442,305-89,709,003 , GRCh38.p12 chr3: 89,393,155-89,659,853 MTATP6P6, MTCO3P6, 3 more genes
    nsv2751487copy number variation1nstd130human GRCh37 chr3: 89,422,868-89,709,003 , GRCh38.p12 chr3: 89,373,718-89,659,853 MTCO1P6, MTCO2P6, 3 more genes
    nsv1326614copy number variation1nstd122human NCBI36 chr3: 89,701,717-89,760,524 , GRCh37.p13 chr3: 89,619,027-89,677,834 , GRCh38.p12 chr3: 89,569,877-89,628,684 MTATP6P6, MTCO2P6, 2 more genes
    nsv1151638inversion1nstd107human GRCh37 chr3: 75,558,505-125,549,112 , GRCh38.p12 chr3: 75,509,354-125,830,269 , ADCY5, 575 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