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 351

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095102copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,348,719-81,396,236 , GRCh38.p12 chr16: 81,315,114-81,362,631 GAN
    nsv7095048copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,348,719-81,348,905 , GRCh38.p12 chr16: 81,315,114-81,315,300 GAN
    nsv7075185inversion1nstd229human GRCh38 chr16: 81,253,947-81,403,619 , GRCh37.p13 chr16: 81,287,552-81,437,224 MIR4720, GAN, 1 more genes
    nsv7072039inversion1nstd229human GRCh38 chr16: 79,903,600-82,537,648 , GRCh37.p13 chr16: 79,937,497-82,571,253 RN7SKP176, LOC105371357, 34 more genes
    nsv7070808inversion1nstd229human GRCh38 chr16: 79,903,594-82,532,651 , GRCh37.p13 chr16: 79,937,491-82,566,256 DYNLRB2, RNU6-1191P, 34 more genes
    nsv7069467inversion1nstd229human GRCh38 chr16: 77,603,047-81,438,175 , GRCh37.p13 chr16: 77,636,944-81,471,780 ATMIN, WWOX, 39 more genes
    nsv7064784inversion1nstd229human GRCh38 chr16: 81,326,019-81,334,027 , GRCh37.p13 chr16: 81,359,624-81,367,632 GAN
    nsv6997620copy number variation1nstd229human GRCh38 chr16: 81,377,066-81,420,033 , GRCh37.p13 chr16: 81,410,671-81,453,638 GAN, MIR4720
    nsv6996784copy number variation1nstd229human GRCh38 chr16: 81,250,634-81,327,749 , GRCh37.p13 chr16: 81,284,239-81,361,354 GAN, BCO1
    nsv6996423copy number variation1nstd229human GRCh38 chr16: 81,338,537-81,340,720 , GRCh37.p13 chr16: 81,372,142-81,374,325 GAN
    nsv6995252copy number variation1nstd229human GRCh38 chr16: 81,386,316-81,394,317 , GRCh37.p13 chr16: 81,419,921-81,427,922 GAN
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6992043copy number variation1nstd229human GRCh38 chr16: 81,383,522-81,394,205 , GRCh37.p13 chr16: 81,417,127-81,427,810 GAN, MIR4720
    nsv6991976copy number variation1nstd229human GRCh38 chr16: 81,324,985-81,328,948 , GRCh37.p13 chr16: 81,358,590-81,362,553 GAN
    nsv6991906copy number variation1nstd229human GRCh38 chr16: 81,359,800-81,413,185 , GRCh37.p13 chr16: 81,393,405-81,446,790 MIR4720, GAN
    nsv6989869copy number variation1nstd229human GRCh38 chr16: 81,327,616-81,327,644 , GRCh37.p13 chr16: 81,361,221-81,361,249 GAN
    nsv6989650copy number variation1nstd229human GRCh38 chr16: 81,368,538-81,377,855 , GRCh37.p13 chr16: 81,402,143-81,411,460 GAN
    nsv6989574copy number variation1nstd229human GRCh38 chr16: 81,358,074-81,706,386 , GRCh37.p13 chr16: 81,391,679-81,739,991 MIR4720, LOC105371362, 6 more genes
    nsv6988787copy number variation1nstd229human GRCh38 chr16: 81,335,436-81,345,992 , GRCh37.p13 chr16: 81,369,041-81,379,597 GAN
    nsv6988029copy number variation1nstd229human GRCh38 chr16: 81,281,416-81,324,626 , GRCh37.p13 chr16: 81,315,021-81,358,231 GAN, BCO1
    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