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 125

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5692621mobile element insertion2nstd211human GRCh38 chr7: 124,782,100-124,782,100 , GRCh37.p13 chr7: 124,422,154-124,422,154 LINC03043
    nsv5678345mobile element insertion1nstd211human GRCh38 chr7: 124,785,885-124,785,885 , GRCh37.p13 chr7: 124,425,939-124,425,939 LINC03043
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5406385mobile element insertion1nstd206human GRCh38 chr7: 124,785,885-124,785,936 , GRCh37.p13 chr7: 124,425,939-124,425,990 LINC03043
    nsv5405882mobile element insertion1nstd206human GRCh38 chr7: 124,782,100-124,782,151 , GRCh37.p13 chr7: 124,422,154-124,422,205 LINC03043
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5118808mobile element insertion1nstd203human GRCh38 chr7: 124,782,089-124,782,096 , GRCh37.p13 chr7: 124,422,143-124,422,150 LINC03043
    nsv5102624mobile element insertion1nstd203human GRCh38 chr7: 124,782,083-124,782,100 , GRCh37.p13 chr7: 124,422,137-124,422,154 LINC03043
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968705copy number variation1nstd200human GRCh38 chr7: 124,783,688-124,798,912 , GRCh37.p13 chr7: 124,423,742-124,438,966 LINC03043
    nsv4968704copy number variation1nstd200human GRCh38 chr7: 124,747,012-124,889,819 , GRCh37.p13 chr7: 124,387,066-124,529,873 GPR37, LINC03043, 1 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4549385insertion1nstd166human GRCh37.p13 chr7: 124,425,549-124,425,549 , GRCh38.p12 chr7: 124,785,495-124,785,495 LINC03043
    nsv4525111copy number variation1nstd166human GRCh37.p13 chr7: 124,426,122-124,426,614 , GRCh38.p12 chr7: 124,786,068-124,786,560 LINC03043
    nsv4488485mobile element insertion1nstd166human GRCh37.p13 chr7: 124,422,137-124,422,137 , GRCh38.p12 chr7: 124,782,083-124,782,083 LINC03043
    nsv4487823mobile element insertion1nstd166human GRCh37.p13 chr7: 124,417,283-124,417,283 , GRCh38.p12 chr7: 124,777,229-124,777,229 LINC03043
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 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