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 351

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141918insertion1nstd232human GRCh37.p13 chr5: 148,929,746-148,929,746 , GRCh38.p12 chr5: 149,550,183-149,550,183 CSNK1A1, ARHGEF37
    nsv7097513copy number variation1nstd102humanUncertain significance GRCh37 chr5: 147,774,340-149,681,936 , GRCh38.p12 chr5: 148,394,777-150,302,373 CSNK1A1, SLC26A2, 39 more genes
    nsv7055117inversion1nstd229human GRCh38 chr5: 149,587,148-149,587,166 , GRCh37.p13 chr5: 148,966,711-148,966,729 ARHGEF37
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7053024inversion1nstd229human GRCh38 chr5: 149,593,927-149,606,868 , GRCh37.p13 chr5: 148,973,490-148,986,431 RNU6-588P, ARHGEF37
    nsv7046154inversion1nstd229human GRCh38 chr5: 149,619,660-149,621,956 , GRCh37.p13 chr5: 148,999,223-149,001,519 ARHGEF37
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6796549copy number variation1nstd229human GRCh38 chr5: 149,611,842-149,668,423 , GRCh37.p13 chr5: 148,991,405-149,047,986 ARHGEF37
    nsv6795896copy number variation1nstd229human GRCh38 chr5: 149,588,678-149,594,109 , GRCh37.p13 chr5: 148,968,241-148,973,672 ARHGEF37
    nsv6795614copy number variation1nstd229human GRCh38 chr5: 149,599,573-149,606,359 , GRCh37.p13 chr5: 148,979,136-148,985,922 RNU6-588P, ARHGEF37
    nsv6795340copy number variation1nstd229human GRCh38 chr5: 149,559,136-149,562,931 , GRCh37.p13 chr5: 148,938,699-148,942,494 ARHGEF37
    nsv6791711copy number variation1nstd229human GRCh38 chr5: 149,626,370-149,640,801 , GRCh37.p13 chr5: 149,005,933-149,020,364 ARHGEF37
    nsv6790255copy number variation1nstd229human GRCh38 chr5: 149,537,031-149,550,058 , GRCh37.p13 chr5: 148,916,594-148,929,621 RPL29P14, ARHGEF37, 1 more genes
    nsv6790143copy number variation1nstd229human GRCh38 chr5: 149,592,401-149,600,100 , GRCh37.p13 chr5: 148,971,964-148,979,663 ARHGEF37
    nsv6789422copy number variation1nstd229human GRCh38 chr5: 149,598,612-149,699,114 , GRCh37.p13 chr5: 148,978,175-149,078,677 ARHGEF37, RNU6-588P
    nsv6788911copy number variation1nstd229human GRCh38 chr5: 149,576,423-149,580,262 , GRCh37.p13 chr5: 148,955,986-148,959,825 ARHGEF37
    nsv6787934copy number variation1nstd229human GRCh38 chr5: 149,573,391-149,573,654 , GRCh37.p13 chr5: 148,952,954-148,953,217 ARHGEF37
    nsv6787153copy number variation1nstd229human GRCh38 chr5: 149,577,709-149,577,923 , GRCh37.p13 chr5: 148,957,272-148,957,486 ARHGEF37
    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