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 93

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057899inversion1nstd229human GRCh38 chr3: 32,727,416-33,178,209 , GRCh37.p13 chr3: 32,768,908-33,219,701 TRIM71, TMPPE, 11 more genes
    nsv7046617inversion1nstd229human GRCh38 chr3: 32,574,554-33,118,910 , GRCh37.p13 chr3: 32,616,046-33,160,402 GLB1, LOC107986072, 12 more genes
    nsv6713249copy number variation1nstd229human GRCh38 chr3: 32,942,344-32,960,826 , GRCh37.p13 chr3: 32,983,836-33,002,318 CCR4
    nsv6547906inversion1nstd223human GRCh38 chr3: 32,955,245-32,955,740 , GRCh37.p13 chr3: 32,996,737-32,997,232 CCR4
    nsv6538982inversion1nstd223human GRCh38 chr3: 32,956,042-32,957,477 , GRCh37.p13 chr3: 32,997,534-32,998,969 CCR4
    nsv6370300copy number variation1nstd223human GRCh38 chr3: 32,955,856-32,956,690 , GRCh37.p13 chr3: 32,997,348-32,998,182 CCR4
    nsv6368059copy number variation1nstd223human GRCh38 chr3: 32,949,269-32,958,109 , GRCh37.p13 chr3: 32,990,761-32,999,601 CCR4
    nsv6355867copy number variation1nstd223human GRCh38 chr3: 32,939,236-32,986,336 , GRCh37.p13 chr3: 32,980,728-33,027,828 CCR4
    nsv6313891copy number variation1nstd102humanUncertain significance GRCh37 chr3: 31,859,973-33,127,072 , GRCh38.p12 chr3: 31,818,481-33,085,580 RPL30P4, RPL21P40, 22 more genes
    nsv6313757copy number variation1nstd102humanUncertain significance GRCh37 chr3: 32,699,328-35,286,114 , GRCh38.p12 chr3: 32,657,836-35,244,622 CRTAP, FECHP1, 26 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv5072217mobile element insertion1nstd203human GRCh38 chr3: 32,956,175-32,956,221 , GRCh37.p13 chr3: 32,997,667-32,997,713 CCR4
    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
    nsv4806494copy number variation1nstd200human GRCh37 chr3: 32,989,977-32,993,027 , GRCh38.p12 chr3: 32,948,485-32,951,535 CCR4
    nsv4793920copy number variation1nstd200human GRCh37 chr3: 32,391,980-33,567,070 , GRCh38.p12 chr3: 32,350,488-33,525,578 , RPL30P4, 25 more genes
    nsv4596427copy number variation1nstd183human GRCh37 chr3: 32,975,755-32,997,774 , GRCh38.p12 chr3: 32,934,263-32,956,282 CCR4
    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