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 808

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137809insertion1nstd102humanBenign GRCh38 chr10: 29,494,839-29,494,839 , GRCh37 chr10: 29,783,768-29,783,768 SVIL
    nsv6126659insertion1nstd186human GRCh37 chr10: 30,018,613-30,018,651 , GRCh38.p12 chr10: 29,729,684-29,729,722 SVIL
    nsv5966678insertion1nstd209human GRCh38 chr10: 29,729,671-29,729,671 , GRCh37.p13 chr10: 30,018,600-30,018,600 SVIL
    nsv5965838insertion1nstd209human GRCh38 chr10: 29,522,093-29,522,093 , GRCh37.p13 chr10: 29,811,022-29,811,022 SVIL
    nsv5963037insertion1nstd209human GRCh38 chr10: 29,494,839-29,494,839 , GRCh37.p13 chr10: 29,783,768-29,783,768 SVIL
    nsv5925469copy number variation1nstd209human GRCh38 chr10: 29,463,917-29,463,985 , GRCh37.p13 chr10: 29,752,846-29,752,914 SVIL-AS1, SVIL
    nsv5924958copy number variation1nstd209human GRCh38 chr10: 29,594,280-29,594,334 , GRCh37.p13 chr10: 29,883,209-29,883,263 SVIL
    nsv5920746copy number variation1nstd209human GRCh38 chr10: 29,654,204-29,654,408 , GRCh37.p13 chr10: 29,943,133-29,943,337 SVIL
    nsv5914543copy number variation1nstd209human GRCh38 chr10: 29,560,699-29,561,353 , GRCh37.p13 chr10: 29,849,628-29,850,282 SVIL
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5911848copy number variation1nstd209human GRCh38 chr10: 29,711,134-29,711,860 , GRCh37.p13 chr10: 30,000,063-30,000,789 RNU6-908P, SVIL
    nsv5911107copy number variation1nstd209human GRCh38 chr10: 29,506,656-29,506,745 , GRCh37.p13 chr10: 29,795,585-29,795,674 SVIL
    nsv5908952copy number variation1nstd209human GRCh38 chr10: 29,629,592-29,630,061 , GRCh37.p13 chr10: 29,918,521-29,918,990 SVIL
    nsv5709360mobile element insertion2nstd211human GRCh38 chr10: 29,651,284-29,651,284 , GRCh37.p13 chr10: 29,940,213-29,940,213 SVIL
    nsv5698912mobile element insertion2nstd211human GRCh38 chr10: 29,522,105-29,522,105 , GRCh37.p13 chr10: 29,811,034-29,811,034 SVIL
    nsv5643932insertion1nstd207human GRCh38 chr10: 29,729,671-29,729,671 , GRCh37.p13 chr10: 30,018,600-30,018,600 SVIL
    nsv5642744insertion1nstd207human GRCh38 chr10: 29,697,181-29,697,181 , GRCh37.p13 chr10: 29,986,110-29,986,110 CKS1BP2, SVIL
    nsv5640413insertion1nstd207human GRCh38 chr10: 29,494,839-29,494,839 , GRCh37.p13 chr10: 29,783,768-29,783,768 SVIL
    nsv5639714insertion1nstd207human GRCh38 chr10: 29,711,431-29,711,431 , GRCh37.p13 chr10: 30,000,360-30,000,360 SVIL, RNU6-908P
    nsv5635681insertion1nstd207human GRCh38 chr10: 29,695,861-29,695,861 , GRCh37.p13 chr10: 29,984,790-29,984,790 SVIL
    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