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 267

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094214copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,383,207-4,409,175 , GRCh38.p12 chr12: 4,274,041-4,300,009 CCND2-AS1, CCND2
    nsv7094213copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-4,796,274 , GRCh38.p12 chr12: 4,259,186-4,687,108 RPS15P7, RAD51AP1, 11 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7094046copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-5,155,155 , GRCh38.p12 chr12: 4,259,186-5,045,989 RPS15P7, CCND2, 18 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068624inversion1nstd229human GRCh38 chr12: 2,500,360-5,372,895 , GRCh37.p13 chr12: 2,609,526-5,482,061 LOC105369607, IQSEC3P1, 62 more genes
    nsv7067673inversion1nstd229human GRCh38 chr12: 4,264,356-4,363,276 , GRCh37.p13 chr12: 4,373,522-4,472,442 RPS15P7, CCND2-AS1, 2 more genes
    nsv6933385copy number variation1nstd229human GRCh38 chr12: 4,281,243-4,281,577 , GRCh37.p13 chr12: 4,390,409-4,390,743 CCND2
    nsv6932736copy number variation1nstd229human GRCh38 chr12: 4,269,913-4,271,960 , GRCh37.p13 chr12: 4,379,079-4,381,126 CCND2-AS1, CCND2
    nsv6932415copy number variation1nstd229human GRCh38 chr12: 4,291,148-4,291,227 , GRCh37.p13 chr12: 4,400,314-4,400,393 CCND2
    nsv6925515copy number variation1nstd229human GRCh38 chr12: 4,279,595-4,280,164 , GRCh37.p13 chr12: 4,388,761-4,389,330 CCND2
    nsv6919650copy number variation1nstd229human GRCh38 chr12: 4,276,801-4,279,500 , GRCh37.p13 chr12: 4,385,967-4,388,666 CCND2
    nsv6913746copy number variation1nstd229human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 LOC101901829, LOC100420673, 29 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6473617copy number variation1nstd223human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 KCNA5, LINC02443, 29 more genes
    nsv6461083copy number variation1nstd223human GRCh38 chr12: 4,279,595-4,280,164 , GRCh37.p13 chr12: 4,388,761-4,389,330 CCND2
    nsv6313933copy number variation1nstd102humanPathogenic GRCh37 chr12: 2,790,077-5,325,700 , GRCh38.p12 chr12: 2,680,911-5,216,534 OTUD4P1, DYRK4, 59 more genes
    nsv6309478copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-4,479,969 , GRCh38.p12 chr12: 4,259,186-4,370,803 CCND2, CCND2-AS1, 3 more genes
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 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