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 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5993616copy number variation1nstd212human GRCh38 chr3: 48,988,771-48,988,976 , GRCh37.p13 chr3: 49,026,204-49,026,409 P4HTM
    nsv5993497copy number variation1nstd212human GRCh38 chr3: 48,992,736-48,992,792 , GRCh37.p13 chr3: 49,030,169-49,030,225 P4HTM
    nsv5993496copy number variation1nstd212human GRCh38 chr3: 48,987,421-48,988,641 , GRCh37.p13 chr3: 49,024,854-49,026,074 P4HTM
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5211134copy number variation1nstd204human GRCh38.p13 chr3: 48,639,801-49,381,300 , GRCh37.p13 chr3: 48,677,234-49,418,733 MIR6890, IHO1, 31 more genes
    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
    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
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 APEH, MIR5193, 90 more genes
    nsv4674083copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,346,677-49,630,228 , GRCh38.p12 chr3: 48,305,187-49,592,795 MIR6823, NCKIPSD, 59 more genes
    nsv4566009mobile element insertion1nstd166human GRCh37.p13 chr3: 49,025,540-49,025,540 , GRCh38.p12 chr3: 48,988,107-48,988,107 P4HTM
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 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