U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 872

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6963490copy number variation1nstd229human GRCh38 chr15: 28,925,767-29,012,254 , GRCh37.p13 chr15: 29,217,970-29,304,457 APBA2
    nsv6969156copy number variation1nstd229human GRCh38 chr15: 28,965,401-29,035,800 , GRCh37.p13 chr15: 29,257,604-29,328,003 APBA2
    nsv6976743copy number variation1nstd229human GRCh38 chr15: 28,974,611-28,991,266 , GRCh37.p13 chr15: 29,266,814-29,283,469 APBA2
    nsv6974373copy number variation1nstd229human GRCh38 chr15: 29,034,250-29,048,711 , GRCh37.p13 chr15: 29,326,453-29,340,914 APBA2
    nsv6961399copy number variation1nstd229human GRCh38 chr15: 28,931,200-28,945,531 , GRCh37.p13 chr15: 29,223,403-29,237,734 APBA2
    nsv6974647copy number variation1nstd229human GRCh38 chr15: 29,049,140-29,060,899 , GRCh37.p13 chr15: 29,341,343-29,353,102 APBA2
    nsv6975998copy number variation1nstd229human GRCh38 chr15: 28,889,506-28,900,470 , GRCh37.p13 chr15: 29,134,652-29,145,616 APBA2
    nsv6975392copy number variation1nstd229human GRCh38 chr15: 28,946,420-28,955,316 , GRCh37.p13 chr15: 29,238,623-29,247,519 APBA2
    nsv6963308copy number variation1nstd229human GRCh38 chr15: 28,888,341-28,893,381 , GRCh37.p13 chr15: 29,133,487-29,138,527 APBA2
    nsv6967589copy number variation1nstd229human GRCh38 chr15: 29,034,383-29,038,566 , GRCh37.p13 chr15: 29,326,586-29,330,769 APBA2
    nsv6976632copy number variation1nstd229human GRCh38 chr15: 28,961,344-28,965,054 , GRCh37.p13 chr15: 29,253,547-29,257,257 APBA2
    nsv6960935copy number variation1nstd229human GRCh38 chr15: 29,076,901-29,079,800 , GRCh37.p13 chr15: 29,369,104-29,372,003 APBA2
    nsv6958314copy number variation1nstd229human GRCh38 chr15: 29,056,143-29,059,037 , GRCh37.p13 chr15: 29,348,346-29,351,240 APBA2
    nsv6974889copy number variation1nstd229human GRCh38 chr15: 28,881,838-28,884,634 , GRCh37.p13 chr15: 29,126,984-29,129,780 APBA2
    nsv6958943copy number variation1nstd229human GRCh38 chr15: 28,925,001-28,926,700 , GRCh37.p13 chr15: 29,217,204-29,218,903 APBA2
    nsv6974666copy number variation1nstd229human GRCh38 chr15: 28,969,151-28,969,184 , GRCh37.p13 chr15: 29,261,354-29,261,387 APBA2
    nsv6511621copy number variation1nstd223human GRCh38 chr15: 28,946,877-28,951,872 , GRCh37.p13 chr15: 29,239,080-29,244,075 APBA2
    nsv6501932copy number variation1nstd223human GRCh38 chr15: 28,964,801-28,967,300 , GRCh37.p13 chr15: 29,257,004-29,259,503 APBA2
    nsv6501274copy number variation1nstd223human GRCh38 chr15: 28,886,977-28,889,430 , GRCh37.p13 chr15: 29,132,123-29,134,576 APBA2
    nsv6505762copy number variation1nstd223human GRCh38 chr15: 29,061,901-29,062,900 , GRCh37.p13 chr15: 29,354,104-29,355,103 APBA2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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