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 415

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906479copy number variation1nstd209human GRCh38 chr2: 203,355,764-203,360,654 , GRCh37.p13 chr2: 204,220,487-204,225,377 ABI2
    nsv5896020copy number variation1nstd209human GRCh38 chr2: 203,423,707-203,425,487 , GRCh37.p13 chr2: 204,288,430-204,290,210 ABI2
    nsv5888191copy number variation1nstd209human GRCh38 chr2: 203,350,297-203,350,777 , GRCh37.p13 chr2: 204,215,020-204,215,500 ABI2
    nsv5887781copy number variation1nstd209human GRCh38 chr2: 203,316,939-203,327,009 , GRCh37.p13 chr2: 204,181,662-204,191,732 ABI2
    nsv5832154copy number variation1nstd209human GRCh38 chr2: 203,355,902-203,360,676 , GRCh37.p13 chr2: 204,220,625-204,225,399 ABI2
    nsv5832153copy number variation2nstd209human GRCh38 chr2: 203,325,727-203,327,026 , GRCh37.p13 chr2: 204,190,450-204,191,749 ABI2
    nsv5831855copy number variation2nstd209human GRCh38 chr2: 203,358,627-203,359,726 , GRCh37.p13 chr2: 204,223,350-204,224,449 ABI2
    nsv5831854copy number variation1nstd209human GRCh38 chr2: 203,316,874-203,327,026 , GRCh37.p13 chr2: 204,181,597-204,191,749 ABI2
    nsv5721344mobile element insertion1nstd211human GRCh38 chr2: 203,405,651-203,405,651 , GRCh37.p13 chr2: 204,270,374-204,270,374 ABI2
    nsv5564843copy number variation1nstd207human GRCh38 chr2: 203,316,939-203,327,009 , GRCh37.p13 chr2: 204,181,662-204,191,732 ABI2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5559677mobile element insertion1nstd206human GRCh38 chr2: 203,405,629-203,405,636 , GRCh37.p13 chr2: 204,270,352-204,270,359 ABI2
    nsv5545951insertion1nstd206human GRCh38 chr2: 203,362,828-203,362,828 , GRCh37.p13 chr2: 204,227,551-204,227,551 TRE-TTC9-1, ABI2
    nsv5544368insertion1nstd206human GRCh38 chr2: 203,393,878-203,393,881 , GRCh37.p13 chr2: 204,258,601-204,258,604 ABI2
    nsv5444797copy number variation1nstd206human GRCh38 chr2: 203,423,712-203,425,449 , GRCh37.p13 chr2: 204,288,435-204,290,172 ABI2
    nsv5436376copy number variation1nstd206human GRCh38 chr2: 203,316,919-203,327,037 , GRCh37.p13 chr2: 204,181,642-204,191,760 ABI2
    nsv5328033translocation1nstd204human GRCh37.p13 chr17: 45,179,128-45,179,128 , GRCh37.p13 chr2: 204,227,552-204,227,552 , GRCh38.p13 chr17: 47,101,762-47,101,762 , GRCh38.p13 chr2: 203,362,829-203,362,829 ABI2, TRE-TTC9-1
    nsv5313924copy number variation1nstd204human GRCh38.p13 chr2: 203,316,854-203,327,091 , GRCh37.p13 chr2: 204,181,577-204,191,814 ABI2
    nsv5212883copy number variation1nstd204human GRCh38.p13 chr2: 203,317,001-203,327,000 , GRCh37.p13 chr2: 204,181,724-204,191,723 ABI2
    nsv5210663copy number variation1nstd204human GRCh38.p13 chr2: 203,317,074-203,327,726 , GRCh37.p13 chr2: 204,181,797-204,192,449 ABI2
    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