U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from BioSystems

Items: 1 to 20 of 20638

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137808copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr19: 49,568,107-49,662,685 , GRCh37 chr19: 50,071,364-50,165,942 IRF3, PRRG2, 4 more genes
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6130807mobile element insertion1nstd186human GRCh37 chr6: 162,181,268-162,181,319 , GRCh38.p12 chr6: 161,760,236-161,760,287 PRKN
    nsv6130409insertion1nstd186human GRCh37 chr12: 132,401,820-132,401,872 , GRCh38.p12 chr12: 131,917,275-131,917,327 ULK1
    nsv6129846insertion1nstd186human GRCh37 chr17: 30,570,449-30,570,449 , GRCh38.p12 chr17: 32,243,430-32,243,430 RHOT1
    nsv6129812mobile element insertion1nstd186human GRCh37 chr22: 18,136,636-18,136,687 , GRCh38.p12 chr22: 17,653,870-17,653,921 BCL2L13
    nsv6129431insertion1nstd186human GRCh37 chr17: 30,565,028-30,565,028 , GRCh38.p12 chr17: 32,238,009-32,238,009 RHOT1
    nsv6129169insertion1nstd186human GRCh37 chr12: 132,401,835-132,401,857 , GRCh38.p12 chr12: 131,917,290-131,917,312 ULK1
    nsv6126721insertion1nstd186human GRCh37 chr4: 87,060,138-87,060,152 , GRCh38.p12 chr4: 86,138,985-86,138,999 MAPK10, MAPK10-AS1
    nsv6126546copy number variation1nstd186human GRCh37 chr22: 18,126,571-18,129,555 , GRCh38.p12 chr22: 17,643,805-17,646,789 BCL2L13
    nsv6124493copy number variation1nstd186human GRCh37 chr17: 46,904,524-46,907,624 , GRCh38.p12 chr17: 48,827,162-48,830,262 CALCOCO2
    nsv6124463copy number variation1nstd186human GRCh37 chr22: 18,141,467-18,144,628 , GRCh38.p12 chr22: 17,658,701-17,661,862 BCL2L13
    nsv6120355copy number variation1nstd186human GRCh37 chr6: 162,583,863-162,586,800 , GRCh38.p12 chr6: 162,162,831-162,165,768 PRKN
    nsv6117757copy number variation1nstd186human GRCh37 chr4: 86,967,178-86,967,682 , GRCh38.p12 chr4: 86,046,025-86,046,529 MAPK10
    nsv6117327mobile element insertion1nstd186human GRCh37 chr6: 162,674,813-162,674,864 , GRCh38.p12 chr6: 162,253,781-162,253,832 PRKN
    nsv6116082copy number variation1nstd186human GRCh37 chr17: 30,505,931-30,507,076 , GRCh38.p12 chr17: 32,178,912-32,180,057 RHOT1
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv6112757copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,056,891-227,164,817 , GRCh38.p12 chr2: 219,192,169-226,300,101 DES, SPEG, 100 more genes
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 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