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 206

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6933029copy number variation1nstd229human GRCh38 chr12: 100,269,016-101,400,896 , GRCh37.p13 chr12: 100,662,794-101,794,674 PIGAP1, SCYL2, 10 more genes
    nsv6930973copy number variation1nstd229human GRCh38 chr12: 100,268,934-100,358,348 , GRCh37.p13 chr12: 100,662,712-100,752,126 SCYL2, SLC17A8
    nsv6930112copy number variation1nstd229human GRCh38 chr12: 100,415,354-100,418,207 , GRCh37.p13 chr12: 100,809,132-100,811,985 SLC17A8
    nsv6925792copy number variation1nstd229human GRCh38 chr12: 100,389,765-100,394,535 , GRCh37.p13 chr12: 100,783,543-100,788,313 SLC17A8
    nsv6923699copy number variation1nstd229human GRCh38 chr12: 100,342,056-100,358,886 , GRCh37.p13 chr12: 100,735,834-100,752,664 SLC17A8, SCYL2
    nsv6923683copy number variation1nstd229human GRCh38 chr12: 100,410,004-100,412,845 , GRCh37.p13 chr12: 100,803,782-100,806,623 SLC17A8
    nsv6923067copy number variation1nstd229human GRCh38 chr12: 100,326,101-100,522,200 , GRCh37.p13 chr12: 100,719,879-100,915,978 NR1H4, SLC17A8, 1 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6590976inversion1nstd223human GRCh38 chr12: 100,363,560-100,363,814 , GRCh37.p13 chr12: 100,757,338-100,757,592 SLC17A8
    nsv6590860inversion1nstd223human GRCh38 chr12: 100,399,071-100,399,790 , GRCh37.p13 chr12: 100,792,849-100,793,568 SLC17A8
    nsv6455799copy number variation1nstd223human GRCh38 chr12: 100,361,261-100,362,769 , GRCh37.p13 chr12: 100,755,039-100,756,547 SLC17A8
    nsv6313913copy number variation1nstd102humanUncertain significance GRCh37 chr12: 100,564,593-103,021,075 , GRCh38.p12 chr12: 100,170,815-102,627,297 DEPDC4, SLC5A8, 46 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132132copy number variation1nstd213human GRCh37 chr12: 100,600,000-101,840,001 , GRCh38.p12 chr12: 100,206,222-101,446,223 ARL1, PIGAP1, 14 more genes
    nsv6092821insertion1nstd212human GRCh38 chr12: 100,407,138-100,407,138 , GRCh37.p13 chr12: 100,800,916-100,800,916 SLC17A8
    nsv5504955copy number variation1nstd206human GRCh38 chr12: 100,407,077-100,407,153 , GRCh37.p13 chr12: 100,800,855-100,800,931 SLC17A8
    nsv5498911copy number variation1nstd206human GRCh38 chr12: 100,351,051-100,364,353 , GRCh37.p13 chr12: 100,744,829-100,758,131 SLC17A8
    nsv5495264copy number variation1nstd206human GRCh38 chr12: 100,369,229-100,369,763 , GRCh37.p13 chr12: 100,763,007-100,763,541 SLC17A8
    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