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 228

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5436241copy number variation1nstd206human GRCh38 chr3: 19,987,330-19,987,651 , GRCh37.p13 chr3: 20,028,822-20,029,143 PP2D1
    nsv5389413copy number variation1nstd186human GRCh37 chr3: 20,038,370-20,038,807 , GRCh38.p12 chr3: 19,996,878-19,997,315 RNU4-85P, PP2D1
    nsv5387675copy number variation1nstd186human GRCh37 chr3: 20,038,371-20,038,807 , GRCh38.p12 chr3: 19,996,879-19,997,315 RNU4-85P, PP2D1
    nsv5351497translocation1nstd200human GRCh38 chr3: 19,983,854-19,983,854 , GRCh38 chr3: 19,983,962-19,983,962 , GRCh37.p13 chr3: 20,025,454-20,025,454 , GRCh37.p13 chr3: 20,025,346-20,025,346 RAB5A, PP2D1
    nsv5343549translocation1nstd200human GRCh37 chr3: 20,025,346-20,025,346 , GRCh37 chr3: 20,025,454-20,025,454 , GRCh38.p12 chr3: 19,983,962-19,983,962 , GRCh38.p12 chr3: 19,983,854-19,983,854 PP2D1, RAB5A
    nsv5314436copy number variation1nstd204human GRCh38.p13 chr3: 19,996,310-19,997,836 , GRCh37.p13 chr3: 20,037,802-20,039,328 RNU4-85P, PP2D1
    nsv5209887copy number variation1nstd204human GRCh38.p13 chr3: 19,977,626-19,979,741 , GRCh37.p13 chr3: 20,019,118-20,021,233 RAB5A, PP2D1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924227copy number variation1nstd200human GRCh38 chr3: 19,996,815-19,997,376 , GRCh37.p13 chr3: 20,038,307-20,038,868 RNU4-85P, PP2D1
    nsv4924226copy number variation1nstd200human GRCh38 chr3: 19,977,058-19,990,869 , GRCh37.p13 chr3: 20,018,550-20,032,361 PP2D1, RAB5A
    nsv4924225copy number variation1nstd200human GRCh38 chr3: 19,967,264-20,074,983 , GRCh37.p13 chr3: 20,008,756-20,116,475 KAT2B, RPL39P18, 4 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4793872copy number variation1nstd200human GRCh37 chr3: 20,038,367-20,038,809 , GRCh38.p12 chr3: 19,996,875-19,997,317 RNU4-85P, PP2D1
    nsv4585644copy number variation1nstd183human GRCh37 chr3: 19,535,653-20,638,501 , GRCh38.p12 chr3: 19,494,161-20,597,009 , RPL39P18, 16 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
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 RPL15, SGO1, 71 more genes
    nsv4451821copy number variation1nstd102humanUncertain significance GRCh37 chr3: 19,833,713-20,933,527 , GRCh38.p12 chr3: 19,792,221-20,892,035 SGO1-AS1, RNY4P22, 13 more genes
    nsv4090108copy number variation1nstd166human GRCh37.p13 chr3: 20,052,009-20,060,227 , GRCh38.p12 chr3: 20,010,517-20,018,735 PP2D1, RPL39P18
    nsv4086254copy number variation1nstd166human GRCh37.p13 chr3: 20,028,822-20,029,143 , GRCh38.p12 chr3: 19,987,330-19,987,651 PP2D1
    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