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 106

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7048271inversion1nstd229human GRCh38 chr3: 59,959,176-65,947,271 , GRCh37.p13 chr3: 59,944,902-65,932,946 LOC105377124, RPS10P10, 63 more genes
    nsv7039673inversion1nstd229human GRCh38 chr3: 59,959,184-65,957,254 , GRCh37.p13 chr3: 59,944,910-65,942,929 PPIAP70, LOC105377114, 63 more genes
    nsv6717345copy number variation1nstd229human GRCh38 chr3: 64,082,101-64,107,300 , GRCh37.p13 chr3: 64,067,777-64,092,976 LINC00994, PRICKLE2-AS1, 2 more genes
    nsv6290933copy number variation1nstd102humanPathogenic GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004 NDUFB4P1, UBA3, 110 more genes
    nsv6134821copy number variation1nstd213human GRCh37 chr3: 63,570,000-64,090,001 , GRCh38.p12 chr3: 63,584,324-64,104,325 ATXN7, PSMD6, 14 more genes
    nsv6134701copy number variation1nstd213human GRCh37 chr3: 63,610,000-66,170,001 , GRCh38.p12 chr3: 63,624,324-66,184,326 ATXN7, MAGI1, 36 more genes
    nsv6134696copy number variation1nstd213human GRCh37 chr3: 60,070,000-66,170,001 , GRCh38.p12 chr3: 60,084,274-66,184,326 FHIT, PTPRG, 65 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924497copy number variation1nstd200human GRCh38 chr3: 64,024,208-64,111,704 , GRCh37.p13 chr3: 64,009,884-64,097,380 , PRICKLE2, 5 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
    nsv4794040copy number variation1nstd200human GRCh37 chr3: 64,009,884-64,097,380 , GRCh38.p12 chr3: 64,024,208-64,111,704 , PRICKLE2, 5 more genes
    nsv4674306copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,449,667-65,561,638 , GRCh38.p12 chr3: 60,463,934-65,575,963 THOC7-AS1, LOC105377647, 56 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
    nsv4559330sequence alteration1nstd166human GRCh37.p13 chr3: 64,091,136-64,091,969 , GRCh38.p12 chr3: 64,105,460-64,106,293 PRICKLE2, PRICKLE2-AS2
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv4080901copy number variation1nstd166human GRCh37.p13 chr3: 64,090,267-64,099,769 , GRCh38.p12 chr3: 64,104,591-64,114,093 PRICKLE2, PRICKLE2-AS2
    nsv3922383copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,956,521-68,514,983 , NCBI36 chr3: 61,931,561-68,597,673 , GRCh38 chr3: 61,970,847-68,465,832 UBL5P3, PRICKLE2-DT, 73 more genes
    nsv3920449copy number variation1nstd102humanUncertain significance GRCh38 chr3: 63,822,831-64,433,817 , NCBI36 chr3: 63,783,547-64,394,533 , GRCh37 chr3: 63,808,507-64,419,493 ATXN7, THOC7, 12 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