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 458

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968604inversion1nstd209human GRCh38 chr2: 49,436,021-59,087,697 , GRCh37.p13 chr2: 49,663,159-59,314,832 , ACYP2, 95 more genes
    nsv5875479copy number variation1nstd209human GRCh38 chr2: 56,313,831-56,313,890 , GRCh37.p13 chr2: 56,540,966-56,541,025 CCDC85A
    nsv5873601copy number variation1nstd209human GRCh38 chr2: 56,247,153-56,252,395 , GRCh37.p13 chr2: 56,474,288-56,479,530 CCDC85A
    nsv5872169copy number variation1nstd209human GRCh38 chr2: 56,244,845-56,250,886 , GRCh37.p13 chr2: 56,471,980-56,478,021 CCDC85A
    nsv5869726copy number variation1nstd209human GRCh38 chr2: 56,265,378-56,265,436 , GRCh37.p13 chr2: 56,492,513-56,492,571 CCDC85A
    nsv5869354copy number variation1nstd209human GRCh38 chr2: 56,294,242-56,294,632 , GRCh37.p13 chr2: 56,521,377-56,521,767 CCDC85A
    nsv5833632copy number variation1nstd209human GRCh38 chr2: 56,244,793-56,247,192 , GRCh37.p13 chr2: 56,471,928-56,474,327 CCDC85A
    nsv5690685mobile element insertion1nstd211human GRCh38 chr2: 56,325,188-56,325,188 , GRCh37.p13 chr2: 56,552,323-56,552,323 CCDC85A
    nsv5687869mobile element insertion1nstd211human GRCh38 chr2: 56,200,816-56,200,816 , GRCh37.p13 chr2: 56,427,951-56,427,951 CCDC85A
    nsv5684878mobile element insertion2nstd211human GRCh38 chr2: 56,307,550-56,307,550 , GRCh37.p13 chr2: 56,534,685-56,534,685 CCDC85A
    nsv5676206mobile element insertion2nstd211human GRCh38 chr2: 56,218,267-56,218,267 , GRCh37.p13 chr2: 56,445,402-56,445,402 CCDC85A
    nsv5614446insertion1nstd207human GRCh38 chr2: 56,313,831-56,313,831 , GRCh37.p13 chr2: 56,540,966-56,540,966 CCDC85A
    nsv5566455copy number variation1nstd207human GRCh38 chr2: 56,265,378-56,265,436 , GRCh37.p13 chr2: 56,492,513-56,492,571 CCDC85A
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5451471copy number variation1nstd206human GRCh38 chr2: 56,251,795-56,251,876 , GRCh37.p13 chr2: 56,478,930-56,479,011 CCDC85A
    nsv5450470copy number variation1nstd206human GRCh38 chr2: 56,213,193-56,213,414 , GRCh37.p13 chr2: 56,440,328-56,440,549 CCDC85A
    nsv5449438copy number variation1nstd206human GRCh38 chr2: 56,234,383-56,237,113 , GRCh37.p13 chr2: 56,461,518-56,464,248 RNA5SP93, CCDC85A
    nsv5447425copy number variation1nstd206human GRCh38 chr2: 56,310,378-56,314,001 , GRCh37.p13 chr2: 56,537,513-56,541,136 CCDC85A
    nsv5437394copy number variation1nstd206human GRCh38 chr2: 56,362,285-56,362,831 , GRCh37.p13 chr2: 56,589,420-56,589,966 CCDC85A
    nsv5434757copy number variation1nstd206human GRCh38 chr2: 56,359,681-56,363,088 , GRCh37.p13 chr2: 56,586,816-56,590,223 CCDC85A
    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