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 749

    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
    nsv7057805inversion1nstd229human GRCh38 chr7: 144,229,946-144,388,138 , GRCh37.p13 chr7: 143,927,039-144,085,231 OR2A42, OR2A9P, 8 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
    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
    nsv6315434copy number variation1nstd102humanUncertain significance GRCh37 chr7: 143,425,718-144,075,390 , GRCh38.p12 chr7|NW_018654715.1: 1-409,704 , GRCh38.p12 chr7: 143,728,625-144,378,297 ARHGEF5, ARHGEF34P, 41 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRBJ2-7, PRSS2, 341 more genes
    nsv6135973copy number variation1nstd213human GRCh37 chr7: 143,430,000-143,940,001 , GRCh38.p12 chr7: 143,732,907-144,242,908 , GRCh38.p12 chr7|NW_018654714.1: 277,226-589,656 OR2A15P, TCAF2P1, 29 more genes
    nsv6135902copy number variation1nstd213human GRCh37 chr7: 143,790,000-143,950,001 , GRCh38.p12 chr7: 144,092,907-144,252,908 ARHGEF35-AS1, OR2A14, 11 more genes
    nsv6135901copy number variation1nstd213human GRCh37 chr7: 143,560,000-143,950,001 , GRCh38.p12 chr7: 143,862,907-144,252,908 , GRCh38.p12 chr7|NW_018654715.1: 1-207,502 OR2Q1P, OR2A5, 23 more genes
    nsv6135570copy number variation1nstd213human GRCh37 chr7: 143,570,000-143,930,001 , GRCh38.p12 chr7: 143,872,907-144,232,908 , GRCh38.p12 chr7|NW_018654715.1: 1-187,502 OR6B1, OR2A41P, 21 more genes
    nsv6116903copy number variation1nstd186human GRCh37 chr7: 143,889,897-144,073,897 , GRCh38.p12 chr7: 144,192,804-144,376,804 , ARHGEF35-AS1, 10 more genes
    nsv6016252copy number variation1nstd212human GRCh38 chr7: 144,180,403-144,377,283 , GRCh37.p13 chr7: 143,877,496-144,074,376 , OR2A1, 11 more genes
    nsv5664740inversion1nstd207human GRCh37.p13 chr7: 143,918,614-144,003,793 , GRCh38 chr7: 144,221,521-144,306,700 OR2A7, OR2A20P, 6 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5414316copy number variation1nstd206human GRCh38 chr7: 144,192,804-144,376,804 , GRCh37.p13 chr7: 143,889,897-144,073,897 , OR2A42, 10 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