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 294

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967788inversion1nstd209human GRCh38 chr1: 46,899,171-47,068,433 , GRCh37.p13 chr1: 47,364,843-47,534,105 CYP4A11, CYP4Z2P, 6 more genes
    nsv5868541copy number variation1nstd209human GRCh38 chr1: 47,041,379-47,060,031 , GRCh37.p13 chr1: 47,507,051-47,525,703 CYP4X1, CYP4Z1
    nsv5830346copy number variation1nstd209human GRCh38 chr1: 47,053,446-47,069,390 , GRCh37.p13 chr1: 47,519,118-47,535,062 CYP4X1, CYP4Z1
    nsv5830041copy number variation1nstd209human GRCh38 chr1: 47,076,942-47,078,345 , GRCh37.p13 chr1: 47,542,614-47,544,017 CYP4Z1
    nsv5830040copy number variation2nstd209human GRCh38 chr1: 47,068,137-47,069,640 , GRCh37.p13 chr1: 47,533,809-47,535,312 CYP4Z1
    nsv5671840inversion1nstd207human GRCh38 chr1: 46,870,366-47,099,487 , GRCh37.p13 chr1: 47,336,038-47,565,159 CYP4A11, CYP4Z2P, 8 more genes
    nsv5612934insertion1nstd207human GRCh38 chr1: 47,118,427-47,118,427 , GRCh37.p13 chr1: 47,584,099-47,584,099 CYP4Z1
    nsv5611927insertion1nstd207human GRCh38 chr1: 47,104,918-47,104,918 , GRCh37.p13 chr1: 47,570,590-47,570,590 CYP4Z1
    nsv5609335insertion1nstd207human GRCh38 chr1: 47,105,774-47,105,774 , GRCh37.p13 chr1: 47,571,446-47,571,446 CYP4Z1
    nsv5607320insertion1nstd207human GRCh38 chr1: 47,097,386-47,097,386 , GRCh37.p13 chr1: 47,563,058-47,563,058 CYP4Z1
    nsv5606863insertion1nstd207human GRCh38 chr1: 47,099,485-47,099,485 , GRCh37.p13 chr1: 47,565,157-47,565,157 CYP4Z1
    nsv5583226copy number variation1nstd207human GRCh38 chr1: 47,104,906-47,104,997 , GRCh37.p13 chr1: 47,570,578-47,570,669 CYP4Z1
    nsv5573726copy number variation1nstd207human GRCh38 chr1: 47,076,549-47,076,859 , GRCh37.p13 chr1: 47,542,221-47,542,531 CYP4Z1
    nsv5566060copy number variation1nstd207human GRCh38 chr1: 47,100,632-47,100,749 , GRCh37.p13 chr1: 47,566,304-47,566,421 CYP4Z1
    nsv5565514copy number variation1nstd207human GRCh38 chr1: 47,118,401-47,118,455 , GRCh37.p13 chr1: 47,584,073-47,584,127 CYP4Z1
    nsv5433744copy number variation1nstd206human GRCh38 chr1: 47,055,835-47,078,835 , GRCh37.p13 chr1: 47,521,507-47,544,507 TUBAP9, CYP4Z1, 1 more genes
    nsv5426098copy number variation1nstd206human GRCh38 chr1: 47,041,379-47,060,035 , GRCh37.p13 chr1: 47,507,051-47,525,707 CYP4Z1, CYP4X1
    nsv5425990copy number variation1nstd206human GRCh38 chr1: 47,085,835-47,091,835 , GRCh37.p13 chr1: 47,551,507-47,557,507 CYP4Z1
    nsv5425747copy number variation1nstd206human GRCh38 chr1: 47,069,835-47,125,835 , GRCh37.p13 chr1: 47,535,507-47,591,507 CYP4Z1, TUBAP9
    nsv5425607copy number variation1nstd206human GRCh38 chr1: 47,071,835-47,080,300 , GRCh37.p13 chr1: 47,537,507-47,545,972 CYP4Z1, TUBAP9
    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