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 844

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968909inversion1nstd209human GRCh38 chr4: 184,990,077-186,324,974 , GRCh37.p13 chr4: 185,911,231-187,246,128 SLC25A4, F11, 25 more genes
    nsv5947965insertion1nstd209human GRCh38 chr4: 186,103,426-186,103,426 , GRCh37.p13 chr4: 187,024,580-187,024,580 FAM149A
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5903072copy number variation1nstd209human GRCh38 chr4: 186,008,703-186,213,064 , GRCh37.p13 chr4: 186,929,857-187,134,218 TLR3, FAM149A, 5 more genes
    nsv5891469copy number variation1nstd209human GRCh38 chr4: 186,172,453-186,176,964 , GRCh37.p13 chr4: 187,093,607-187,098,118 FAM149A
    nsv5839079copy number variation1nstd209human GRCh38 chr4: 186,113,876-186,116,969 , GRCh37.p13 chr4: 187,035,030-187,038,123 FAM149A
    nsv5838821copy number variation1nstd209human GRCh38 chr4: 186,076,599-186,113,014 , GRCh37.p13 chr4: 186,997,753-187,034,168 FAM149A, TLR3
    nsv5838219copy number variation2nstd209human GRCh38 chr4: 186,172,313-186,177,042 , GRCh37.p13 chr4: 187,093,467-187,098,196 FAM149A
    nsv5673650copy number variation1nstd102humanPathogenic GRCh37 chr4: 186,997,774-187,630,981 , GRCh38.p12 chr4: 186,076,620-186,709,827 FLJ38576, SLC25A5P6, 13 more genes
    nsv5628232insertion1nstd207human GRCh38 chr4: 186,173,400-186,173,400 , GRCh37.p13 chr4: 187,094,554-187,094,554 FAM149A
    nsv5625623insertion1nstd207human GRCh38 chr4: 186,136,964-186,136,964 , GRCh37.p13 chr4: 187,058,118-187,058,118 FAM149A
    nsv5576784copy number variation1nstd207human GRCh38 chr4: 186,172,333-186,173,376 , GRCh37.p13 chr4: 187,093,487-187,094,530 FAM149A
    nsv5566208copy number variation1nstd207human GRCh38 chr4: 186,173,467-186,177,076 , GRCh37.p13 chr4: 187,094,621-187,098,230 FAM149A
    nsv5473075copy number variation1nstd206human GRCh38 chr4: 186,105,403-186,105,495 , GRCh37.p13 chr4: 187,026,557-187,026,649 FAM149A
    nsv5469850copy number variation1nstd206human GRCh38 chr4: 186,136,804-186,136,887 , GRCh37.p13 chr4: 187,057,958-187,058,041 FAM149A
    nsv5461382copy number variation1nstd206human GRCh38 chr4: 186,158,607-186,158,703 , GRCh37.p13 chr4: 187,079,761-187,079,857 FAM149A, RPSAP70
    nsv5460777copy number variation1nstd206human GRCh38 chr4: 186,150,540-186,150,888 , GRCh37.p13 chr4: 187,071,694-187,072,042 FAM149A
    nsv5459185copy number variation1nstd206human GRCh38 chr4: 186,172,125-186,177,087 , GRCh37.p13 chr4: 187,093,279-187,098,241 FAM149A
    nsv5395595mobile element insertion1nstd206human GRCh38 chr4: 186,172,333-186,172,384 , GRCh37.p13 chr4: 187,093,487-187,093,538 FAM149A
    nsv5387325copy number variation2nstd186human GRCh37 chr4: 187,093,487-187,098,237 , GRCh38.p12 chr4: 186,172,333-186,177,083 FAM149A
    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