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 181

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095972copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,520,044-220,986,760 , GRCh38.p12 chr1: 218,346,702-220,813,418 TGFB2, LOC105373475, 38 more genes
    nsv6677980copy number variation1nstd229human GRCh38 chr1: 218,472,541-218,576,193 , GRCh37.p13 chr1: 218,645,883-218,749,535 LINC02869
    nsv6673695copy number variation1nstd229human GRCh38 chr1: 218,519,380-218,520,081 , GRCh37.p13 chr1: 218,692,722-218,693,423 LINC02869
    nsv6672825copy number variation1nstd229human GRCh38 chr1: 218,525,811-218,528,494 , GRCh37.p13 chr1: 218,699,153-218,701,836 LINC02869
    nsv6671903copy number variation1nstd229human GRCh38 chr1: 218,109,001-218,591,300 , GRCh37.p13 chr1: 218,282,343-218,764,642 LINC02869, RPS26P17, 6 more genes
    nsv6671231copy number variation1nstd229human GRCh38 chr1: 218,513,697-218,526,793 , GRCh37.p13 chr1: 218,687,039-218,700,135 LINC02869
    nsv6658816copy number variation1nstd229human GRCh38 chr1: 218,481,501-218,509,300 , GRCh37.p13 chr1: 218,654,843-218,682,642 LINC02869
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6334528copy number variation1nstd223human GRCh38 chr1: 218,504,971-218,513,789 , GRCh37.p13 chr1: 218,678,313-218,687,131 LINC02869
    nsv6290633copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,589,671-219,026,274 , GRCh38.p12 chr1: 217,416,329-218,852,932 LINC01653, SPATA17-AS1, 15 more genes
    nsv6290612copy number variation1nstd102humanPathogenic GRCh37 chr1: 216,243,817-220,231,236 , GRCh38.p12 chr1: 216,070,475-220,057,894 LINC00210, LOC107985281, 36 more genes
    nsv6290569copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,199,578-223,035,427 , GRCh38.p12 chr1: 215,026,235-222,862,085 SPATA17, BROX, 97 more genes
    nsv6290478copy number variation1nstd102humanPathogenic GRCh37 chr1: 217,219,510-219,385,296 , GRCh38.p12 chr1: 217,046,168-219,211,954 ESRRG, TGFB2, 22 more genes
    nsv6290398copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,238,773-219,024,035 , GRCh38.p12 chr1: 218,065,431-218,850,693 TGFB2, RRP15, 8 more genes
    nsv6133857copy number variation1nstd213human GRCh37 chr1: 215,920,000-223,130,001 , GRCh38.p12 chr1: 215,746,658-222,956,659 BPNT1, HHIPL2, 95 more genes
    nsv6133641copy number variation1nstd213human GRCh37 chr1: 218,650,000-218,830,001 , GRCh38.p12 chr1: 218,476,658-218,656,659 LINC02869
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 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