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 882

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966166insertion1nstd209human GRCh38 chr1: 243,845,405-243,845,405 , GRCh37.p13 chr1: 244,008,707-244,008,707 AKT3
    nsv5963404insertion1nstd209human GRCh38 chr1: 243,525,804-243,525,804 , GRCh37.p13 chr1: 243,689,106-243,689,106 AKT3
    nsv5887512copy number variation1nstd209human GRCh38 chr1: 243,619,443-243,620,456 , GRCh37.p13 chr1: 243,782,745-243,783,758 AKT3
    nsv5884551copy number variation1nstd209human GRCh38 chr1: 243,806,742-243,820,376 , GRCh37.p13 chr1: 243,970,044-243,983,678 AKT3
    nsv5882911copy number variation1nstd209human GRCh38 chr1: 243,609,747-243,609,870 , GRCh37.p13 chr1: 243,773,049-243,773,172 AKT3
    nsv5881659copy number variation1nstd209human GRCh38 chr1: 243,673,501-243,674,415 , GRCh37.p13 chr1: 243,836,803-243,837,717 AKT3
    nsv5872682copy number variation1nstd209human GRCh38 chr1: 243,699,323-243,699,510 , GRCh37.p13 chr1: 243,862,625-243,862,812 AKT3
    nsv5869469copy number variation1nstd209human GRCh38 chr1: 243,532,106-243,536,019 , GRCh37.p13 chr1: 243,695,408-243,699,321 AKT3
    nsv5829763copy number variation1nstd209human GRCh38 chr1: 243,619,485-243,620,484 , GRCh37.p13 chr1: 243,782,787-243,783,786 AKT3
    nsv5829762copy number variation1nstd209human GRCh38 chr1: 243,532,050-243,536,049 , GRCh37.p13 chr1: 243,695,352-243,699,351 AKT3
    nsv5829290copy number variation1nstd209human GRCh38 chr1: 243,830,799-243,833,248 , GRCh37.p13 chr1: 243,994,101-243,996,550 AKT3
    nsv5829289copy number variation1nstd209human GRCh38 chr1: 243,806,716-243,813,272 , GRCh37.p13 chr1: 243,970,018-243,976,574 AKT3
    nsv5719776mobile element insertion2nstd211human GRCh38 chr1: 243,682,332-243,682,332 , GRCh37.p13 chr1: 243,845,634-243,845,634 AKT3
    nsv5682419mobile element insertion1nstd211human GRCh38 chr1: 243,835,830-243,835,830 , GRCh37.p13 chr1: 243,999,132-243,999,132 AKT3
    nsv5676923mobile element insertion2nstd211human GRCh38 chr1: 243,833,460-243,833,460 , GRCh37.p13 chr1: 243,996,762-243,996,762 AKT3
    nsv5674236copy number variation1nstd102humanUncertain significance GRCh38 chr1: 243,433,667-243,744,233 , GRCh37.p13 chr1: 243,596,969-243,907,535 AKT3, FABP7P1, 1 more genes
    nsv5673172copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 243,652,316-243,652,442 , GRCh38.p12 chr1: 243,489,014-243,489,140 , GRCh38.p12 chr1|NT_187519.1: 501,122-501,248 AKT3, SDCCAG8
    nsv5622861insertion1nstd207human GRCh38 chr1: 243,845,405-243,845,405 , GRCh37.p13 chr1: 244,008,707-244,008,707 AKT3
    nsv5616548insertion1nstd207human GRCh38 chr1: 243,525,831-243,525,831 , GRCh37.p13 chr1: 243,689,133-243,689,133 AKT3
    nsv5614713insertion1nstd207human GRCh38 chr1: 243,525,837-243,525,837 , GRCh37.p13 chr1: 243,689,139-243,689,139 AKT3
    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