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 211

    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
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv6835157copy number variation1nstd229human GRCh38 chr7: 155,586,961-156,721,504 , GRCh37.p13 chr7: 155,379,656-156,514,198 LOC105375597, RBM33, 15 more genes
    nsv6832162copy number variation1nstd229human GRCh38 chr7: 156,432,148-156,435,844 , GRCh37.p13 chr7: 156,224,842-156,228,538 LOC105375599, LOC285889
    nsv6824525copy number variation1nstd229human GRCh38 chr7: 152,687,878-156,500,924 , GRCh37.p13 chr7: 152,384,963-156,293,618 RN7SKP280, LINC03010, 44 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
    nsv6634318copy number variation1nstd102humanPathogenic GRCh38 chr7: 156,350,691-156,939,511 , GRCh37.p13 chr7: 156,143,385-156,732,205 LOC105375604, LINC00244, 10 more genes
    nsv6315450copy number variation1nstd102humanPathogenic GRCh37 chr7: 155,389,460-157,960,969 , GRCh38.p12 chr7: 155,596,766-158,168,277 RNF32, MIR153-2, 38 more genes
    nsv6315413copy number variation1nstd102humanPathogenic GRCh37 chr7: 154,831,466-156,356,088 , GRCh38.p12 chr7: 155,039,756-156,563,394 SHH, INSIG1, 27 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6315172copy number variation1nstd102humanPathogenic GRCh37 chr7: 149,062,717-159,124,131 , GRCh38.p12 chr7: 149,365,626-159,331,441 KCNH2, SLC4A2, 191 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
    nsv6312335copy number variation1nstd102humanUncertain significance GRCh37 chr7: 155,595,594-157,208,792 , GRCh38.p12 chr7: 155,802,900-157,416,098 LOC105375602, RNU4-31P, 28 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
    nsv6136977copy number variation1nstd213human GRCh37 chr7: 155,830,000-159,138,663 , GRCh38.p12 chr7: 156,037,306-159,335,973 DNAJB6, LMBR1, 44 more genes
    nsv6135980copy number variation1nstd213human GRCh37 chr7: 154,380,000-159,138,663 , GRCh38.p12 chr7: 154,588,290-159,335,973 DPP6, INSIG1, 71 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