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 121

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5529215copy number variation1nstd206human GRCh38 chr16: 31,036,080-31,041,965 , GRCh37.p13 chr16: 31,047,401-31,053,286 LOC101928762, STX4
    nsv5331270translocation1nstd200human GRCh37 chr16: 31,047,401-31,047,401 , GRCh37 chr16: 31,053,286-31,053,286 , GRCh38.p12 chr16: 31,041,965-31,041,965 , GRCh38.p12 chr16: 31,036,080-31,036,080 LOC101928762, STX4
    nsv5303620copy number variation1nstd204human GRCh37.p13 chr16: 31,047,396-31,053,288 , GRCh38.p13 chr16: 31,036,075-31,041,967 STX4, LOC101928762
    nsv5272199copy number variation1nstd204human GRCh38.p13 chr16: 31,036,268-31,037,617 , GRCh37.p13 chr16: 31,047,589-31,048,938 STX4
    nsv5266770copy number variation1nstd204human GRCh38.p13 chr16: 31,036,818-31,037,963 , GRCh37.p13 chr16: 31,048,139-31,049,284 STX4
    nsv5265040copy number variation1nstd204human GRCh38.p13 chr16: 31,036,018-31,042,604 , GRCh37.p13 chr16: 31,047,339-31,053,925 LOC101928762, STX4
    nsv5261648copy number variation1nstd204human GRCh38.p13 chr16: 31,031,218-31,033,342 , GRCh37.p13 chr16: 31,042,539-31,044,663 STX4
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv5003516copy number variation1nstd200human GRCh38 chr16: 31,036,080-31,041,965 , GRCh37.p13 chr16: 31,047,401-31,053,286 LOC101928762, STX4
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4864101copy number variation1nstd200human GRCh37 chr16: 31,034,645-31,082,946 , GRCh38.p12 chr16: 31,023,324-31,071,625 ZNF668, STX4, 1 more genes
    nsv4856834copy number variation1nstd200human GRCh37 chr16: 31,041,003-31,042,969 , GRCh38.p12 chr16: 31,029,682-31,031,648 STX4
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4625270copy number variation1nstd183human GRCh37 chr16: 31,036,936-31,075,708 , GRCh38.p12 chr16: 31,025,615-31,064,387 STX4, LOC101928762, 1 more genes
    nsv4621302copy number variation1nstd183human GRCh37 chr16: 31,044,290-31,046,534 , GRCh38.p12 chr16: 31,032,969-31,035,213 STX4
    nsv4620172copy number variation1nstd183human GRCh37 chr16: 31,036,765-31,080,356 , GRCh38.p12 chr16: 31,025,444-31,069,035 STX4, LOC101928762, 1 more genes
    nsv4455315copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,851,860-31,156,762 , GRCh38.p12 chr16: 30,840,539-31,145,441 LOC101928762, ZNF646, 20 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 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