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 108

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6995426copy number variation1nstd229human GRCh38 chr16: 31,088,601-31,099,800 , GRCh37.p13 chr16: 31,099,922-31,111,121 PRSS53, VKORC1
    nsv6992677copy number variation1nstd229human GRCh38 chr16: 30,859,398-31,135,376 , GRCh37.p13 chr16: 30,870,719-31,146,697 SETD1A, HSD3B7, 19 more genes
    nsv6990871copy number variation1nstd229human GRCh38 chr16: 30,902,101-31,224,500 , GRCh37.p13 chr16: 30,913,422-31,235,821 CTF2P, VKORC1, 22 more genes
    nsv6984006copy number variation1nstd229human GRCh38 chr16: 31,093,293-31,093,623 , GRCh37.p13 chr16: 31,104,614-31,104,944 VKORC1
    nsv6983575copy number variation1nstd229human GRCh38 chr16: 31,084,383-31,089,905 , GRCh37.p13 chr16: 31,095,704-31,101,226 VKORC1, ZNF646, 1 more genes
    nsv6978565copy number variation1nstd229human GRCh38 chr16: 31,093,701-31,099,000 , GRCh37.p13 chr16: 31,105,022-31,110,321 VKORC1
    nsv6623598copy number variation1nstd224human GRCh37 chr16: 31,072,600-31,104,509 , GRCh38.p12 chr16: 31,061,279-31,093,188 VKORC1, PRSS53, 2 more genes
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6509248copy number variation1nstd223human GRCh38 chr16: 31,090,704-31,092,129 , GRCh37.p13 chr16: 31,102,025-31,103,450 VKORC1
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133022copy number variation1nstd213human GRCh37 chr16: 30,300,000-32,030,001 , GRCh38.p12 chr16: 30,288,679-32,018,680 COX6A2, CTF1, 91 more genes
    nsv5358084translocation1nstd200human GRCh38 chr16: 31,091,120-31,091,120 , GRCh38 chr16: 31,090,843-31,090,843 , GRCh37.p13 chr16: 31,102,441-31,102,441 , GRCh37.p13 chr16: 31,102,164-31,102,164 VKORC1
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    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
    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
    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