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 107

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057841inversion1nstd229human GRCh38 chr7: 130,366,667-130,370,793 , GRCh37.p13 chr7: 130,006,508-130,010,634 , GRCh37.p13 chr7|NW_003871065.1: 22,085-26,211 LOC105375504, CPA5
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6828831copy number variation1nstd229human GRCh38 chr7: 130,353,801-130,364,700 , GRCh37.p13 chr7|NW_003871065.1: 9,219-20,118 , GRCh37.p13 chr7: 129,993,642-130,004,541 CPA5, LOC105375504
    nsv6636929copy number variation1nstd102humanUncertain significance GRCh37 chr7: 129,147,455-132,777,678 , GRCh38.p12 chr7: 129,507,614-133,092,918 LINC03008, TMEM209, 60 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
    nsv6560945inversion1nstd223human GRCh38 chr7: 129,758,099-137,582,370 , GRCh37.p13 chr7: 129,397,939-137,267,116 LOC100506937, SLC35B4, 115 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6313722copy number variation1nstd102humanPathogenic GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221 IRF5, MIR129-1, 153 more genes
    nsv6135963copy number variation1nstd213human GRCh37 chr7: 129,900,000-130,020,001 , GRCh38.p12 chr7: 130,260,160-130,380,160 CPA1, CPA2, 4 more genes
    nsv6135554copy number variation1nstd213human GRCh37 chr7: 126,190,000-130,150,001 , GRCh38.p12 chr7: 126,549,946-130,510,160 IMPDH1, ODCP, 96 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
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4729643copy number variation1nstd102humanUncertain significance GRCh37 chr7: 129,605,827-133,093,756 , GRCh38.p12 chr7: 129,965,987-133,409,002 LOC100506937, CPA1, 57 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 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