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 99

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5234028copy number variation1nstd204human GRCh38.p13 chr3: 75,085,083-75,121,649 , GRCh37.p13 chr3: 75,134,234-75,170,800 NIPA2P2
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924576copy number variation1nstd200human GRCh38 chr3: 74,437,520-75,450,819 , GRCh37.p13 chr3: 74,486,671-75,499,970 , RN7SL294P, 17 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4794075copy number variation1nstd200human GRCh37 chr3: 74,486,671-75,499,970 , GRCh38.p12 chr3: 74,437,520-75,450,819 , LOC105377167, 17 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4562963mobile element insertion1nstd166human GRCh37.p13 chr3: 75,134,416-75,134,416 , GRCh38.p12 chr3: 75,085,265-75,085,265 NIPA2P2
    nsv4082498copy number variation1nstd166human GRCh37.p13 chr3: 75,107,150-75,273,029 , GRCh38.p12 chr3: 75,057,999-75,223,878 LOC107986099, HNRNPA3P6, 3 more genes
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 more genes
    nsv3920686copy number variation1nstd102humanLikely benign GRCh37 chr3: 74,943,399-75,540,161 , GRCh38 chr3: 74,894,248-75,491,010 , NCBI36 chr3: 75,026,089-75,622,851 LINC02018, OR7E66P, 13 more genes
    nsv3919908copy number variation1nstd102humanBenign GRCh38 chr3: 74,979,514-75,115,565 , NCBI36 chr3: 75,111,355-75,247,406 , GRCh37 chr3: 75,028,665-75,164,716 NIPA2P2
    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
    nsv3913280copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 68,460,820-76,896,160 , GRCh37 chr3: 68,378,130-76,813,470 , GRCh38 chr3: 68,328,980-76,764,319 AKR1B1P2, GPR27, 105 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
    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