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 199

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7046837inversion1nstd229human GRCh38 chr7: 146,996,779-152,901,438 , GRCh37.p13 chr7: 146,693,871-152,598,523 RARRES2, RN7SL76P, 153 more genes
    nsv7039560inversion1nstd229human GRCh38 chr7: 149,238,508-149,284,014 , GRCh37.p13 chr7: 148,935,599-148,981,105 ZNF212, ZNF783, 1 more genes
    nsv6826112copy number variation1nstd229human GRCh38 chr7: 149,249,431-149,250,848 , GRCh37.p13 chr7: 148,946,522-148,947,939 ZNF212
    nsv6825099copy number variation1nstd229human GRCh38 chr7: 149,249,501-149,255,000 , GRCh37.p13 chr7: 148,946,592-148,952,091 ZNF212
    nsv6822551copy number variation1nstd229human GRCh38 chr7: 149,255,701-149,260,500 , GRCh37.p13 chr7: 148,952,792-148,957,591 ZNF783, ZNF212
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6558115inversion1nstd223human GRCh38 chr7: 146,996,771-152,901,398 , GRCh37.p13 chr7: 146,693,863-152,598,483 ZNF398, PRKAG2-AS1, 153 more genes
    nsv6422367copy number variation1nstd223human GRCh38 chr7: 149,228,607-149,243,449 , GRCh37.p13 chr7: 148,925,698-148,940,540 ZNF212
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6315169copy number variation1nstd102humanPathogenic GRCh37 chr7: 146,927,174-159,128,556 , GRCh38.p12 chr7: 147,230,082-159,335,866 LOC105375554, ATP5PBP3, 233 more genes
    nsv6291241copy number variation1nstd102humanPathogenic GRCh37 chr7: 148,153,261-157,543,640 , GRCh38.p12 chr7: 148,456,169-157,750,948 TRC-GCA23-1, HTR5A-AS1, 210 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6290897copy number variation1nstd102humanPathogenic GRCh37 chr7: 148,695,373-159,119,707 , GRCh38.p12 chr7: 148,998,281-159,327,017 TRC-GCA21-1, LINC00996, 209 more genes
    nsv6136972copy number variation1nstd213human GRCh37 chr7: 146,490,000-151,820,001 , GRCh38.p12 chr7: 146,792,908-152,122,916 AOC1, KCNH2, 140 more genes
    nsv6135904copy number variation1nstd213human GRCh37 chr7: 148,450,000-150,420,001 , GRCh38.p12 chr7: 148,752,908-150,722,913 EZH2, RNY3, 78 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