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 115

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5688935mobile element insertion1nstd211human GRCh38 chr2: 99,161,338-99,161,338 , GRCh37.p13 chr2: 99,777,801-99,777,801 MITD1, LIPT1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5448881copy number variation1nstd206human GRCh38 chr2: 99,121,779-99,182,757 , GRCh37.p13 chr2: 99,738,242-99,799,220 LIPT1, MRPL30, 3 more genes
    nsv5077506mobile element insertion1nstd203human GRCh38 chr2: 99,161,251-99,161,292 , GRCh37.p13 chr2: 99,777,714-99,777,755 LIPT1, MITD1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894842copy number variation1nstd200human GRCh38 chr2: 99,121,779-99,182,757 , GRCh37.p13 chr2: 99,738,242-99,799,220 TSGA10, C2orf15, 3 more genes
    nsv4781662copy number variation1nstd200human GRCh37 chr2: 99,738,242-99,799,220 , GRCh38.p12 chr2: 99,121,779-99,182,757 C2orf15, MITD1, 3 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4728703copy number variation1nstd102humanUncertain significance GRCh37 chr2: 99,356,669-99,984,607 , GRCh38.p12 chr2: 98,740,206-99,368,144 LYG2, CRACDL, 14 more genes
    nsv4584468copy number variation1nstd183human GRCh37 chr2: 99,770,961-99,774,563 , GRCh38.p12 chr2: 99,154,498-99,158,100 LIPT1, TSGA10
    nsv4519174copy number variation1nstd166human GRCh37.p13 chr2: 99,724,999-99,864,000 , GRCh38.p12 chr2: 99,108,536-99,247,537 MRPL30, LIPT1, 4 more genes
    nsv4454817copy number variation1nstd102humanUncertain significance GRCh37 chr2: 99,542,665-100,190,293 , GRCh38.p12 chr2: 98,926,202-99,573,831 CRACDL, LYG2, 12 more genes
    nsv4387020copy number variation2nstd173human GRCh37 chr2: 99,738,559-99,794,824 , GRCh38.p12 chr2: 99,122,096-99,178,361 TSGA10, MITD1, 2 more genes
    nsv4325920inversion1nstd166human GRCh37.p13 chr2: 99,617,898-100,469,272 , GRCh38.p12 chr2: 99,001,435-99,852,810 , AFF3, 13 more genes
    nsv4312591inversion1nstd166human GRCh37.p13 chr2: 97,201,014-102,197,203 , GRCh38.p12 chr2: 96,535,277-101,580,741 , CNGA3, 106 more genes
    nsv3931605copy number variation1nstd167human GRCh37 chr2: 99,777,736-99,777,773 , GRCh38.p12 chr2: 99,161,273-99,161,310 LIPT1, MITD1
    nsv3931405copy number variation1nstd167human GRCh37 chr2: 99,777,736-99,777,772 , GRCh38.p12 chr2: 99,161,273-99,161,309 LIPT1, MITD1
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 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