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 958

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141952copy number variation1nstd232human GRCh37.p13 chr6: 1,827,626-1,827,685 , GRCh38.p12 chr6: 1,827,392-1,827,451 GMDS
    nsv7137073copy number variation1nstd102humanPathogenic GRCh37 chr6: 491,126-1,624,775 , GRCh38.p12 chr6: 491,126-1,624,540 RN7SL352P, LOC107986555, 18 more genes
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7057019inversion1nstd229human GRCh38 chr6: 1,714,061-1,733,360 , GRCh37.p13 chr6: 1,714,295-1,733,594 GMDS
    nsv7056557inversion1nstd229human GRCh38 chr6: 1,686,691-1,726,483 , GRCh37.p13 chr6: 1,686,925-1,726,717 GMDS
    nsv7054269inversion1nstd229human GRCh38 chr6: 2,121,231-2,123,429 , GRCh37.p13 chr6: 2,121,465-2,123,663 GMDS
    nsv7048529inversion1nstd229human GRCh38 chr6: 1,913,159-2,085,186 , GRCh37.p13 chr6: 1,913,393-2,085,420 GMDS
    nsv7047357inversion1nstd229human GRCh38 chr6: 1,913,232-2,085,186 , GRCh37.p13 chr6: 1,913,466-2,085,420 GMDS
    nsv7046764inversion1nstd229human GRCh38 chr6: 1,805,635-2,065,593 , GRCh37.p13 chr6: 1,805,869-2,065,827 GMDS
    nsv7046171inversion1nstd229human GRCh38 chr6: 1,731,593-1,738,113 , GRCh37.p13 chr6: 1,731,827-1,738,347 GMDS
    nsv7045038inversion1nstd229human GRCh38 chr6: 2,061,444-2,061,477 , GRCh37.p13 chr6: 2,061,678-2,061,711 GMDS
    nsv7041436inversion1nstd229human GRCh38 chr6: 1,680,887-1,680,930 , GRCh37.p13 chr6: 1,681,121-1,681,164 GMDS
    nsv6797966copy number variation1nstd229human GRCh38 chr6: 1,699,508-1,704,658 , GRCh37.p13 chr6: 1,699,742-1,704,892 GMDS
    nsv6797957copy number variation1nstd229human GRCh38 chr6: 2,045,601-2,080,718 , GRCh37.p13 chr6: 2,045,835-2,080,952 GMDS
    nsv6797858copy number variation1nstd229human GRCh38 chr6: 1,689,624-1,698,176 , GRCh37.p13 chr6: 1,689,858-1,698,410 GMDS
    nsv6797831copy number variation1nstd229human GRCh38 chr6: 1,965,873-2,093,726 , GRCh37.p13 chr6: 1,966,107-2,093,960 GMDS
    nsv6797795copy number variation1nstd229human GRCh38 chr6: 1,808,395-1,811,921 , GRCh37.p13 chr6: 1,808,629-1,812,155 GMDS
    nsv6797736copy number variation1nstd229human GRCh38 chr6: 1,838,548-1,896,590 , GRCh37.p13 chr6: 1,838,782-1,896,824 GMDS
    nsv6797733copy number variation1nstd229human GRCh38 chr6: 1,737,866-1,737,937 , GRCh37.p13 chr6: 1,738,100-1,738,171 GMDS
    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