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 167

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv6744014copy number variation1nstd229human GRCh38 chr4: 119,535,882-120,079,702 , GRCh37.p13 chr4: 120,457,037-121,000,857 MAD2L1, LINC02502, 4 more genes
    nsv6740715copy number variation1nstd229human GRCh38 chr4: 119,780,324-120,960,202 , GRCh37.p13 chr4: 120,701,479-121,881,357 PRDM5, LINC01365, 7 more genes
    nsv6570561inversion1nstd223human GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207 MYOZ2, NT5C3AP1, 109 more genes
    nsv6379332copy number variation1nstd223human GRCh38 chr4: 119,800,101-119,804,069 , GRCh37.p13 chr4: 120,721,256-120,725,224 LINC01365
    nsv6375764copy number variation1nstd223human GRCh38 chr4: 119,799,628-119,800,353 , GRCh37.p13 chr4: 120,720,783-120,721,508 LINC01365
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 LOC105377395, SEPTIN7P14, 152 more genes
    nsv6313717copy number variation1nstd102humanUncertain significance GRCh37 chr4: 119,902,254-121,463,237 , GRCh38.p12 chr4: 118,981,099-120,542,082 LOC102723967, PDE5A, 26 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6255237mobile element insertion1nstd215human GRCh38 chr4: 119,798,941-119,798,941 , GRCh37.p13 chr4: 120,720,096-120,720,096 LINC01365
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv6134722copy number variation1nstd213human GRCh37 chr4: 120,664,424-120,896,935 , GRCh38.p12 chr4: 119,743,269-119,975,780 LINC02502, LINC01365
    nsv6075280insertion1nstd212human GRCh38 chr4: 119,798,931-119,798,931 , GRCh37.p13 chr4: 120,720,086-120,720,086 LINC01365
    nsv5962409insertion1nstd209human GRCh38 chr4: 119,798,931-119,798,931 , GRCh37.p13 chr4: 120,720,086-120,720,086 LINC01365
    nsv5681601mobile element insertion2nstd211human GRCh38 chr4: 119,798,941-119,798,941 , GRCh37.p13 chr4: 120,720,096-120,720,096 LINC01365
    nsv5619465insertion1nstd207human GRCh38 chr4: 119,798,931-119,798,931 , GRCh37.p13 chr4: 120,720,086-120,720,086 LINC01365
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 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