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 304

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098929copy number variation1nstd102humanPathogenic GRCh38 chr3: 195,950,438-197,629,463 , GRCh37.p13 chr3: 195,677,309-197,356,334 LINC01063, RNF168, 52 more genes
    nsv7098781copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,591,052-197,682,644 , GRCh38.p12 chr3: 195,864,181-197,955,773 ZDHHC19, DLG1, 68 more genes
    nsv7055557inversion1nstd229human GRCh38 chr3: 195,655,301-197,630,693 , GRCh37.p13 chr3: 195,382,172-197,357,564 MIR570HG, RN7SL434P, 66 more genes
    nsv7055374inversion1nstd229human GRCh38 chr3: 197,589,239-197,616,212 , GRCh37.p13 chr3: 197,316,110-197,343,083 SDHAP4
    nsv7053064inversion1nstd229human GRCh38 chr3: 197,597,842-197,814,362 , GRCh37.p13 chr3: 197,324,713-197,541,233 MIR922, LOC112268458, 5 more genes
    nsv7051130inversion1nstd229human GRCh38 chr3: 196,923,427-197,979,595 , GRCh37.p13 chr3: 196,650,298-197,706,466 LOC105374310, LINC02012, 29 more genes
    nsv7047164inversion1nstd229human GRCh38 chr3: 196,815,362-197,824,853 , GRCh37.p13 chr3: 196,542,233-197,551,724 DLG1, RUBCN, 24 more genes
    nsv6736886copy number variation1nstd229human GRCh38 chr3: 197,047,829-197,820,647 , GRCh37.p13 chr3: 196,774,700-197,547,518 RPL36P7, MIR4797, 14 more genes
    nsv6733307copy number variation1nstd229human GRCh38 chr3: 197,396,684-198,059,614 , GRCh37.p13 chr3: 197,123,555-197,786,485 IQCG, LMLN-AS1, 19 more genes
    nsv6730375copy number variation1nstd229human GRCh38 chr3: 197,594,423-197,808,007 , GRCh37.p13 chr3: 197,321,294-197,534,878 PPP4R2P4, LRCH3, 5 more genes
    nsv6730005copy number variation1nstd229human GRCh38 chr3: 197,594,879-197,716,235 , GRCh37.p13 chr3: 197,321,750-197,443,106 RUBCN, MIR922, 3 more genes
    nsv6721775copy number variation1nstd229human GRCh38 chr3: 197,283,996-197,843,341 , GRCh37.p13 chr3: 197,010,867-197,570,212 MIR4797, LINC02012, 15 more genes
    nsv6720064copy number variation1nstd229human GRCh38 chr3: 197,394,307-197,957,911 , GRCh37.p13 chr3: 197,121,178-197,684,782 FYTTD1, RNU6-858P, 15 more genes
    nsv6636887copy number variation1nstd102humanPathogenic GRCh37 chr3: 195,690,228-197,356,334 , GRCh38.p12 chr3: 195,963,357-197,629,463 LOC105374307, NRROS, 52 more genes
    nsv6636446copy number variation1nstd102humanUncertain significance GRCh37 chr3: 197,185,584-197,672,964 , GRCh38.p12 chr3: 197,458,713-197,946,093 MIR922, LRCH3, 14 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628941copy number variation1nstd224human GRCh37 chr3: 197,092,657-197,344,036 , GRCh38.p12 chr3: 197,365,786-197,617,165 , GRCh38.p12 chr3|NT_187534.1: 1-162,429 BDH1, SDHAP4, 5 more genes
    nsv6628940copy number variation1nstd224human GRCh37 chr3: 196,876,614-197,346,566 , GRCh38.p12 chr3: 197,149,743-197,619,695 RPL36P7, LOC105374309, 8 more genes
    nsv6628750copy number variation1nstd224human GRCh37 chr3: 197,034,985-197,393,245 , GRCh38.p12 chr3: 197,308,114-197,666,374 BDH1, SDHAP4, 7 more genes
    nsv6628558copy number variation1nstd224human GRCh37 chr3: 197,031,608-197,344,036 , GRCh38.p12 chr3: 197,304,737-197,617,165 , GRCh38.p12 chr3|NT_187534.1: 1-162,429 BDH1, SDHAP4, 6 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