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 161

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888496copy number variation1nstd209human GRCh38 chr3: 87,228,014-87,232,425 , GRCh37.p13 chr3: 87,277,164-87,281,575 CHMP2B
    nsv5453215copy number variation1nstd206human GRCh38 chr3: 87,202,584-87,227,055 , GRCh37.p13 chr3: 87,251,734-87,276,205 CHMP2B, MIR4795
    nsv5333702translocation1nstd200human GRCh37 chr3: 87,281,574-87,281,574 , GRCh37 chr3: 87,277,164-87,277,164 , GRCh38.p12 chr3: 87,228,014-87,228,014 , GRCh38.p12 chr3: 87,232,424-87,232,424 CHMP2B
    nsv5301590copy number variation1nstd204human GRCh38.p13 chr3: 87,202,574-87,227,064 , GRCh37.p13 chr3: 87,251,724-87,276,214 MIR4795, CHMP2B
    nsv5232656copy number variation1nstd204human GRCh38.p13 chr3: 87,202,596-87,228,519 , GRCh37.p13 chr3: 87,251,746-87,277,669 CHMP2B, MIR4795
    nsv4929038copy number variation1nstd200human GRCh38 chr3: 86,784,014-87,815,346 , GRCh37.p13 chr3: 86,833,164-87,864,496 LOC105377196, VGLL3, 12 more genes
    nsv4927695copy number variation1nstd200human GRCh38 chr3: 87,186,577-87,519,943 , GRCh37.p13 chr3: 87,235,727-87,569,093 CHMP2B, POU1F1, 2 more genes
    nsv4924683copy number variation1nstd200human GRCh38 chr3: 87,202,584-87,227,055 , GRCh37.p13 chr3: 87,251,734-87,276,205 CHMP2B, MIR4795
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4794149copy number variation1nstd200human GRCh37 chr3: 87,251,734-87,276,205 , GRCh38.p12 chr3: 87,202,584-87,227,055 CHMP2B, MIR4795
    nsv4674591copy number variation1nstd102humanUncertain significance GRCh37 chr3: 86,841,600-87,862,816 , GRCh38.p12 chr3: 86,792,450-87,813,666 PSMC1P6, LOC105377196, 12 more genes
    nsv4586889copy number variation1nstd183human GRCh37 chr3: 87,253,194-87,275,516 , GRCh38.p12 chr3: 87,204,044-87,226,366 MIR4795, CHMP2B
    nsv4568251inversion1nstd166human GRCh37.p13 chr3: 81,845,861-90,137,796 , GRCh38.p12 chr3: 81,796,710-90,088,646 POU1F1, CHMP2B, 54 more genes
    nsv4567322mobile element insertion1nstd166human GRCh37.p13 chr3: 87,305,154-87,305,154 , GRCh38.p12 chr3: 87,256,004-87,256,004 CHMP2B
    nsv4472288mobile element insertion1nstd166human GRCh37.p13 chr3: 87,298,654-87,298,654 , GRCh38.p12 chr3: 87,249,504-87,249,504 CHMP2B
    nsv4450501copy number variation1nstd102humanUncertain significance GRCh37 chr3: 87,236,925-87,567,548 , GRCh38.p12 chr3: 87,187,775-87,518,398 CHMP2B, POU1F1, 2 more genes
    nsv4379210copy number variation1nstd173human GRCh37 chr3: 87,205,485-89,477,159 , GRCh38.p12 chr3: 87,156,335-89,428,009 ABCF2P1, KRT8P25, 20 more genes
    nsv4373997copy number variation1nstd173human GRCh37 chr3: 87,236,790-87,567,548 , GRCh38.p12 chr3: 87,187,640-87,518,398 KRT8P25, POU1F1, 2 more genes
    nsv4084774copy number variation1nstd166human GRCh37.p13 chr3: 87,283,478-87,293,370 , GRCh38.p12 chr3: 87,234,328-87,244,220 CHMP2B
    nsv3923231copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 76,896,101-89,814,775 , GRCh37 chr3: 76,813,411-89,732,085 , GRCh38 chr3: 76,764,260-89,682,935 EPHA3, GBE1, 80 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