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 208

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074449inversion1nstd229human GRCh38 chr10: 79,521,421-80,234,809 , GRCh37.p13 chr10: 81,281,177-81,994,565 LINC02679, LOC642361, 29 more genes
    nsv7070338inversion1nstd229human GRCh38 chr10: 79,538,419-80,221,732 , GRCh37.p13 chr10: 81,298,175-81,981,488 RPL22P18, BEND3P3, 29 more genes
    nsv7067530inversion1nstd229human GRCh38 chr10: 79,527,707-80,210,201 , GRCh37.p13 chr10: 81,287,463-81,969,957 PGGT1BP2, ZNRF2P3, 28 more genes
    nsv7066359inversion1nstd229human GRCh38 chr10: 79,541,399-80,221,640 , GRCh37.p13 chr10: 81,301,155-81,981,396 SFTPA3P, MBL3P, 29 more genes
    nsv6896866copy number variation1nstd229human GRCh38 chr10: 80,091,600-80,388,756 , GRCh37.p13 chr10: 81,851,356-82,148,512 LINC00857, EIF5AP4, 10 more genes
    nsv6893720copy number variation1nstd229human GRCh38 chr10: 76,896,077-84,570,412 , GRCh37.p13 chr10: 78,655,835-86,330,168 RNU6-129P, LOC105378392, 111 more genes
    nsv6888919copy number variation1nstd229human GRCh38 chr10: 80,179,318-80,273,713 , GRCh37.p13 chr10: 81,939,074-82,033,469 MAT1A, EIF5AP4, 4 more genes
    nsv6880956copy number variation1nstd229human GRCh38 chr10: 80,211,101-80,225,000 , GRCh37.p13 chr10: 81,970,857-81,984,756 LINC00857, RPS12P2
    nsv6638011copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,603,170-81,984,775 , GRCh38.p12 chr10: 79,843,414-80,225,019 DPY19L2P5, CTSLP6, 18 more genes
    nsv6595201inversion1nstd223human GRCh38 chr10: 79,542,962-80,217,143 , GRCh37.p13 chr10: 81,302,718-81,976,899 PGGT1BP2, RPS12P18, 29 more genes
    nsv6587639inversion1nstd223human GRCh38 chr10: 79,533,804-80,226,633 , GRCh37.p13 chr10: 81,293,560-81,986,389 SFTPA2, LINC00857, 29 more genes
    nsv6586915inversion1nstd223human GRCh38 chr10: 79,533,787-80,226,538 , GRCh37.p13 chr10: 81,293,543-81,986,294 SFTPA1, ZNRF2P3, 29 more genes
    nsv6585055inversion1nstd223human GRCh38 chr10: 79,754,380-87,461,415 , GRCh37.p13 chr10: 81,514,136-89,221,172 DYDC2, LOC105378394, 114 more genes
    nsv6575760inversion1nstd223human GRCh38 chr10: 79,538,320-80,221,775 , GRCh37.p13 chr10: 81,298,076-81,981,531 LINC02679, LOC100421010, 29 more genes
    nsv6452391copy number variation1nstd223human GRCh38 chr10: 80,219,601-80,225,800 , GRCh37.p13 chr10: 81,979,357-81,985,556 LINC00857
    nsv6438581copy number variation1nstd223human GRCh38 chr10: 80,219,901-80,260,600 , GRCh37.p13 chr10: 81,979,657-82,020,356 LOC100130698, LINC00857, 1 more genes
    nsv6315478copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,630,468-88,980,961 , GRCh38.p12 chr10: 79,870,712-87,221,204 RNU1-19P, LOC107984187, 102 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