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 176

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954905insertion1nstd209human GRCh38 chr7: 141,703,339-141,703,339 , GRCh37.p13 chr7: 141,403,139-141,403,139 WEE2-AS1
    nsv5921939copy number variation1nstd209human GRCh38 chr7: 141,738,515-141,738,571 , GRCh37.p13 chr7: 141,438,315-141,438,371 SSBP1, WEE2-AS1
    nsv5729411mobile element insertion2nstd211human GRCh38 chr7: 141,703,267-141,703,267 , GRCh37.p13 chr7: 141,403,067-141,403,067 WEE2-AS1
    nsv5635926insertion1nstd207human GRCh38 chr7: 141,703,338-141,703,338 , GRCh37.p13 chr7: 141,403,138-141,403,138 WEE2-AS1
    nsv5578245copy number variation1nstd207human GRCh38 chr7: 141,731,798-141,731,851 , GRCh37.p13 chr7: 141,431,598-141,431,651 WEE2-AS1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5541061insertion1nstd206human GRCh38 chr7: 141,703,339-141,703,339 , GRCh37.p13 chr7: 141,403,139-141,403,139 WEE2-AS1
    nsv5342279translocation1nstd200human GRCh37 chr7: 141,438,372-141,438,372 , GRCh37 chr7: 141,438,316-141,438,316 , GRCh38.p12 chr7: 141,738,516-141,738,516 , GRCh38.p12 chr7|NW_003315922.2: 111,116-111,116 , GRCh38.p12 chr7|NW_003315922.2: 111,172-111,172 , GRCh38.p12 chr7: 141,738,572-141,738,572 SSBP1, WEE2-AS1
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5181637mobile element insertion1nstd203human GRCh38 chr7: 141,714,885-141,714,901 , GRCh37.p13 chr7: 141,414,685-141,414,701 WEE2, WEE2-AS1
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968870copy number variation1nstd200human GRCh38 chr7: 141,708,106-141,708,537 , GRCh37.p13 chr7: 141,407,906-141,408,337 WEE2, WEE2-AS1
    nsv4958745copy number variation1nstd200human GRCh38 chr7: 141,714,720-141,719,001 , GRCh37.p13 chr7: 141,414,520-141,418,801 WEE2, WEE2-AS1
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4869975inversion1nstd200human GRCh37 chr7: 140,214,312-141,993,227 , GRCh38.p12 chr7: 140,514,512-142,288,987 , TMEM178B, 44 more genes
    nsv4825392copy number variation1nstd200human GRCh37 chr7: 141,407,906-141,408,337 , GRCh38.p12 chr7|NW_003315922.2: 80,706-81,137 , GRCh38.p12 chr7: 141,708,106-141,708,537 WEE2, WEE2-AS1
    nsv4768836insertion1nstd186human GRCh37 chr7: 141,403,139-141,403,139 , GRCh38.p12 chr7: 141,703,339-141,703,339 , GRCh38.p12 chr7|NW_003315922.2: 69,934-69,934 WEE2-AS1
    nsv4754204insertion1nstd199human GRCh37 chr7: 141,403,139-141,403,139 , GRCh38.p12 chr7|NW_003315922.2: 69,934-69,934 , GRCh38.p12 chr7: 141,703,339-141,703,339 WEE2-AS1
    nsv4744860copy number variation1nstd199human GRCh37 chr7: 141,431,516-141,431,587 , GRCh38.p12 chr7: 141,731,716-141,731,787 , GRCh38.p12 chr7|NW_003315922.2: 104,316-104,387 WEE2-AS1, WEE2
    nsv4726469mobile element insertion1nstd186human GRCh37 chr7: 141,403,139-141,403,139 , GRCh38.p12 chr7|NW_003315922.2: 69,934-69,934 , GRCh38.p12 chr7: 141,703,339-141,703,339 WEE2-AS1
    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