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 143

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    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
    nsv4927321copy number variation1nstd200human GRCh38 chr3: 71,292,361-71,292,526 , GRCh37.p13 chr3: 71,341,512-71,341,677 FOXP1, FOXP1-AS1
    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
    nsv4796955copy number variation1nstd200human GRCh37 chr3: 71,341,511-71,341,678 , GRCh38.p12 chr3: 71,292,360-71,292,527 FOXP1, FOXP1-AS1
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 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
    nsv4452292copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,339,830-71,389,085 , GRCh38.p12 chr3: 71,290,679-71,339,934 FOXP1, FOXP1-AS1
    nsv3972089copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,319,916-71,564,385 , GRCh38.p12 chr3: 71,270,765-71,515,234 FOXP1, FOXP1-AS1
    nsv3972045copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,161,687-71,591,240 , GRCh38.p12 chr3: 71,112,536-71,542,089 MIR1284, FOXP1, 1 more genes
    nsv3924472copy number variation1nstd102humanUncertain significance NCBI36 chr3: 71,256,348-72,024,108 , GRCh37 chr3: 71,173,658-71,941,418 , GRCh38 chr3: 71,124,507-71,892,267 MIR1284, RN7SL271P, 7 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
    nsv3920193copy number variation1nstd102humanPathogenic GRCh37 chr3: 67,441,430-73,463,152 , NCBI36 chr3: 67,524,120-73,545,842 , GRCh38 chr3: 67,391,006-73,414,001 RNPC3P1, LOC105377162, 65 more genes
    nsv3917061copy number variation1nstd102humanPathogenic NCBI36 chr3: 68,940,430-75,092,800 , GRCh37.p13 chr3: 68,857,740-75,010,110 , GRCh38.p12 chr3: 68,808,589-74,960,959 RYBP, GXYLT2, 69 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
    nsv3915179copy number variation1nstd102humanPathogenic NCBI36 chr3: 71,075,461-71,993,730 , GRCh37 chr3: 70,992,771-71,911,040 , GRCh38 chr3: 70,943,620-71,861,889 GPR27, FOXP1, 7 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
    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