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 75

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv4927737copy number variation1nstd200human GRCh38 chr3: 88,093,089-88,093,273 , GRCh37.p13 chr3: 88,142,239-88,142,423 CBX5P1, CGGBP1, 1 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4728132copy number variation1nstd102humanUncertain significance GRCh37 chr3: 87,877,640-88,214,146 , GRCh38.p12 chr3: 87,828,490-88,164,996 C3orf38, CGGBP1, 4 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
    nsv4379210copy number variation1nstd173human GRCh37 chr3: 87,205,485-89,477,159 , GRCh38.p12 chr3: 87,156,335-89,428,009 ABCF2P1, KRT8P25, 20 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
    nsv3922718copy number variation1nstd102humanLikely benign NCBI36 chr3: 88,166,270-88,966,815 , GRCh37 chr3: 88,083,580-88,884,125 , GRCh38 chr3: 88,034,430-88,834,975 ZNF654, C3orf38, 6 more genes
    nsv3919352copy number variation1nstd102humanUncertain significance NCBI36 chr3: 87,280,527-89,571,391 , GRCh37.p13 chr3: 87,197,837-89,488,701 , GRCh38.p12 chr3: 87,148,687-89,439,551 CSNKA2IP, MIR4795, 20 more genes
    nsv3916669copy number variation1nstd102humanPathogenic NCBI36 chr3: 74,781,223-89,627,521 , GRCh37 chr3: 74,698,533-89,544,831 , GRCh38 chr3: 74,649,382-89,495,681 LOC105377187, LOC101927374, 109 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
    nsv3889348copy number variation1nstd102humanUncertain significance GRCh37 chr3: 87,969,926-88,963,355 , GRCh38.p12 chr3: 87,920,776-88,914,205 HTR1F, ZNF654, 7 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
    nsv3206335copy number variation1nstd152human GRCh38 chr3: 88,087,015-88,161,445 , GRCh37.p13 chr3: 88,136,165-88,210,595 CGGBP1, ZNF654, 2 more genes
    esv4010653copy number variation1estd233human GRCh37 chr3: 87,134,000-88,210,000 , GRCh38.p12 chr3: 87,084,850-88,160,850 HTR1F, POU1F1, 13 more genes
    nsv2190699short tandem repeat1nstd128human GRCh37 chr3: 88,144,029-88,144,043 , GRCh38.p12 chr3: 88,094,879-88,094,893 ZNF654, CGGBP1, 1 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