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 98

    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
    nsv6991338copy number variation1nstd229human GRCh38 chr16: 31,324,840-31,575,158 , GRCh37.p13 chr16: 31,336,161-31,586,479 YBX3P1, COX6A2, 14 more genes
    nsv6980127copy number variation1nstd229human GRCh38 chr16: 31,261,410-31,863,261 , GRCh37.p13 chr16: 31,272,731-31,874,582 ITGAM, FRG2KP, 24 more genes
    nsv6978532copy number variation1nstd229human GRCh38 chr16: 31,525,838-31,562,686 , GRCh37.p13 chr16: 31,537,159-31,574,007 AHSP, VN1R65P, 3 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
    nsv6580010inversion1nstd223human GRCh38 chr16: 31,525,951-31,526,581 , GRCh37.p13 chr16: 31,537,272-31,537,902 AHSP
    nsv6515405copy number variation1nstd223human GRCh38 chr16: 31,471,084-31,594,845 , GRCh37.p13 chr16: 31,482,405-31,606,166 SLC5A2, RUSF1, 7 more genes
    nsv6495869copy number variation1nstd223human GRCh38 chr16: 31,525,861-31,527,320 , GRCh37.p13 chr16: 31,537,182-31,538,641 AHSP
    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
    nsv6132984copy number variation1nstd213human GRCh37 chr16: 31,340,000-32,080,001 , GRCh38.p12 chr16: 31,328,679-32,068,680 COX6A2, ITGAD, 31 more genes
    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
    nsv4856848copy number variation1nstd200human GRCh37 chr16: 31,537,159-31,574,015 , GRCh38.p12 chr16: 31,525,838-31,562,694 VN1R64P, AHSP, 3 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
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4420411copy number variation1nstd174human GRCh37 chr16: 31,526,789-31,822,853 , GRCh38.p12 chr16: 31,515,468-31,811,532 , LINC02190, 14 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 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