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 129

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050122inversion1nstd229human GRCh38 chr3: 72,870,426-72,885,754 , GRCh37.p13 chr3: 72,919,577-72,934,905 PSMD12P1, GXYLT2, 1 more genes
    nsv7041748inversion1nstd229human GRCh38 chr3: 72,070,390-75,778,215 , GRCh37.p13 chr3: 72,119,541-75,827,366 FTH1P23, LOC107986099, 66 more genes
    nsv6715482copy number variation1nstd229human GRCh38 chr3: 72,691,001-72,968,565 , GRCh37.p13 chr3: 72,740,152-73,017,716 LOC105377161, SHQ1, 5 more genes
    nsv6714371copy number variation1nstd229human GRCh38 chr3: 72,821,401-73,061,500 , GRCh37.p13 chr3: 72,870,552-73,110,651 GXYLT2, FTH1P23, 6 more genes
    nsv6712385copy number variation1nstd229human GRCh38 chr3: 66,065,527-73,237,527 , GRCh37.p13 chr3: 66,051,202-73,286,678 , RNA5SP136, 79 more genes
    nsv6368260copy number variation1nstd223human GRCh38 chr3: 72,879,359-72,971,806 , GRCh37.p13 chr3: 72,928,510-73,020,957 FTH1P23, GXYLT2, 1 more genes
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6135027copy number variation1nstd213human GRCh37 chr3: 72,860,000-72,990,001 , GRCh38.p12 chr3: 72,810,849-72,940,850 SHQ1, PSMD12P1, 3 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924566copy number variation1nstd200human GRCh38 chr3: 72,879,321-72,971,813 , GRCh37.p13 chr3: 72,928,472-73,020,964 GXYLT2, FTH1P23, 1 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
    nsv4794068copy number variation1nstd200human GRCh37 chr3: 72,928,498-73,020,965 , GRCh38.p12 chr3: 72,879,347-72,971,814 GXYLT2, FTH1P23, 1 more genes
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 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
    nsv4080049copy number variation1nstd166human GRCh37.p13 chr3: 72,928,499-73,020,964 , GRCh38.p12 chr3: 72,879,348-72,971,813 GXYLT2, LAPTM4BP2, 1 more genes
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 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