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 302

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901847copy number variation1nstd209human GRCh38 chr5: 149,579,656-149,579,956 , GRCh37.p13 chr5: 148,959,219-148,959,519 ARHGEF37
    nsv5724498mobile element insertion2nstd211human GRCh38 chr5: 149,606,554-149,606,554 , GRCh37.p13 chr5: 148,986,117-148,986,117 RNU6-588P, ARHGEF37
    nsv5681092mobile element insertion1nstd211human GRCh38 chr5: 149,577,384-149,577,384 , GRCh37.p13 chr5: 148,956,947-148,956,947 ARHGEF37
    nsv5557459mobile element insertion1nstd206human GRCh38 chr5: 149,606,569-149,606,579 , GRCh37.p13 chr5: 148,986,132-148,986,142 RNU6-588P, ARHGEF37
    nsv5470354copy number variation1nstd206human GRCh38 chr5: 149,619,752-149,620,704 , GRCh37.p13 chr5: 148,999,315-149,000,267 ARHGEF37
    nsv5465077copy number variation1nstd206human GRCh38 chr5: 149,631,460-149,633,443 , GRCh37.p13 chr5: 149,011,023-149,013,006 ARHGEF37
    nsv5465009copy number variation1nstd206human GRCh38 chr5: 149,623,854-149,623,911 , GRCh37.p13 chr5: 149,003,417-149,003,474 ARHGEF37
    nsv5464062copy number variation1nstd206human GRCh38 chr5: 149,570,302-149,570,606 , GRCh37.p13 chr5: 148,949,865-148,950,169 ARHGEF37
    nsv5460649copy number variation1nstd206human GRCh38 chr5: 149,611,842-149,668,426 , GRCh37.p13 chr5: 148,991,405-149,047,989 ARHGEF37
    nsv5229220copy number variation1nstd204human GRCh38.p13 chr5: 149,609,701-149,669,400 , GRCh37.p13 chr5: 148,989,264-149,048,963 ARHGEF37
    nsv5228618copy number variation1nstd204human GRCh38.p13 chr5: 149,550,201-149,557,000 , GRCh37.p13 chr5: 148,929,764-148,936,563 ARHGEF37, CSNK1A1
    nsv5223621copy number variation1nstd204human GRCh38.p13 chr5: 149,630,209-149,664,812 , GRCh37.p13 chr5: 149,009,772-149,044,375 ARHGEF37
    nsv5199630mobile element insertion1nstd203human GRCh38 chr5: 149,624,913-149,624,913 , GRCh37.p13 chr5: 149,004,476-149,004,476 ARHGEF37
    nsv5098993mobile element insertion1nstd203human GRCh38 chr5: 149,587,304-149,587,315 , GRCh37.p13 chr5: 148,966,867-148,966,878 ARHGEF37
    nsv5093567mobile element insertion1nstd203human GRCh38 chr5: 149,587,434-149,587,434 , GRCh37.p13 chr5: 148,966,997-148,966,997 ARHGEF37
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4949081copy number variation1nstd200human GRCh38 chr5: 149,626,370-149,640,801 , GRCh37.p13 chr5: 149,005,933-149,020,364 ARHGEF37
    nsv4949080copy number variation1nstd200human GRCh38 chr5: 149,588,021-149,588,462 , GRCh37.p13 chr5: 148,967,584-148,968,025 ARHGEF37
    nsv4949079copy number variation1nstd200human GRCh38 chr5: 149,585,660-149,590,534 , GRCh37.p13 chr5: 148,965,223-148,970,097 ARHGEF37
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 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