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 167

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975022inversion1nstd209human GRCh38 chr7: 34,818,028-37,653,165 , GRCh37.p13 chr7: 34,857,640-37,692,768 , AOAH, 41 more genes
    nsv5968440inversion1nstd209human GRCh38 chr7: 36,375,001-36,383,362 , GRCh37.p13 chr7: 36,414,610-36,422,971 MATCAP2
    nsv5958774insertion1nstd209human GRCh38 chr7: 36,337,098-36,337,098 , GRCh37.p13 chr7: 36,376,707-36,376,707 MATCAP2
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 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
    nsv5480211copy number variation1nstd206human GRCh38 chr7: 36,345,472-36,345,578 , GRCh37.p13 chr7: 36,385,081-36,385,187 MATCAP2
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966183copy number variation1nstd200human GRCh38 chr7: 36,377,086-36,380,771 , GRCh37.p13 chr7: 36,416,695-36,420,380 MATCAP2
    nsv4966182copy number variation1nstd200human GRCh38 chr7: 36,346,893-36,353,523 , GRCh37.p13 chr7: 36,386,502-36,393,132 MATCAP2
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4731451copy number variation1nstd199human GRCh37 chr7: 36,383,007-36,383,061 , GRCh38.p12 chr7: 36,343,398-36,343,452 MATCAP2
    nsv4494963mobile element insertion1nstd166human GRCh37.p13 chr7: 36,383,661-36,383,661 , GRCh38.p12 chr7: 36,344,052-36,344,052 MATCAP2
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4150329copy number variation1nstd166human GRCh37.p13 chr7: 36,394,144-36,394,218 , GRCh38.p12 chr7: 36,354,535-36,354,609 MATCAP2
    nsv4137100copy number variation1nstd166human GRCh37.p13 chr7: 36,410,367-36,410,747 , GRCh38.p12 chr7: 36,370,758-36,371,138 MATCAP2
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 MMD2, ICA1-AS1, 554 more genes
    nsv3917263copy number variation1nstd102humanPathogenic GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334 MIR4649, LOC107986794, 444 more genes
    nsv3915802copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008 RPL23AP52, IQCE, 638 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