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 141

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054819inversion1nstd229human GRCh38 chr5: 112,393,108-116,183,657 , GRCh37.p13 chr5: 111,728,805-115,519,354 SRP19, LINCADL, 53 more genes
    nsv7047000inversion1nstd229human GRCh38 chr5: 112,427,651-114,848,458 , GRCh37.p13 chr5: 111,763,348-114,184,155 XBP1P1, SRP19, 23 more genes
    nsv6776157copy number variation1nstd229human GRCh38 chr5: 112,570,201-112,667,200 , GRCh37.p13 chr5: 111,905,898-112,002,897 LOC102467216, LINC02200
    nsv6773859copy number variation1nstd229human GRCh38 chr5: 112,309,501-113,522,200 , GRCh37.p13 chr5: 111,645,198-112,857,897 LOC105379123, APC, 19 more genes
    nsv6768034copy number variation1nstd229human GRCh38 chr5: 112,631,160-112,634,193 , GRCh37.p13 chr5: 111,966,857-111,969,890 LINC02200
    nsv6763798copy number variation1nstd229human GRCh38 chr5: 111,959,103-112,732,497 , GRCh37.p13 chr5: 111,294,800-112,068,194 EPB41L4A-DT, LINC02200, 10 more genes
    nsv6762826copy number variation1nstd229human GRCh38 chr5: 112,061,006-112,699,809 , GRCh37.p13 chr5: 111,396,703-112,035,506 TMEM183AP6, LOC102467216, 7 more genes
    nsv6760008copy number variation1nstd229human GRCh38 chr5: 112,619,743-112,645,334 , GRCh37.p13 chr5: 111,955,440-111,981,031 LINC02200
    nsv6400014copy number variation1nstd223human GRCh38 chr5: 112,085,398-112,780,300 , GRCh37.p13 chr5: 111,421,095-112,115,997 EPB41L4A-AS1, TMEM183AP6, 10 more genes
    nsv6313709copy number variation1nstd102humanPathogenic GRCh37 chr5: 111,676,467-113,755,797 , GRCh38.p12 chr5: 112,340,770-114,420,100 APC, TSSK1B, 23 more genes
    nsv6313698copy number variation1nstd102humanPathogenic GRCh37 chr5: 111,443,783-116,255,660 , GRCh38.p12 chr5: 112,108,086-116,919,964 RPS17P2, COMMD10, 71 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6135689copy number variation1nstd213human GRCh37 chr5: 96,670,000-113,570,001 , GRCh38.p12 chr5: 97,334,296-114,234,304 APC, CAMK4, 154 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6134969copy number variation1nstd213human GRCh37 chr5: 111,840,000-112,290,001 , GRCh38.p12 chr5: 112,504,303-112,954,304 APC, SRP19, 9 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 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