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 1595

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148121copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,284,269-51,870,080 , GRCh38.p12 chr10: 45,788,821-50,110,320 LOC100420617, ZNF488, 108 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
    nsv7098865copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr10|NW_003871068.1: 1-2,281,126 , GRCh38 chr10: 45,704,708-50,015,268 , GRCh37.p13 chr10: 46,200,156-51,028,871 CHAT, CTSLP2, 107 more genes
    nsv7093389copy number variation1nstd102humanUncertain significance GRCh37 chr10: 46,584,432-51,974,628 , GRCh38.p12 chr10: 45,931,517-50,214,868 NCOA4, AGAP7P, 106 more genes
    nsv7066519inversion1nstd229human GRCh38 chr10: 45,802,941-50,026,843 , GRCh37.p13 chr10|NW_003871068.1: 74,056-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,028,871 RNA5SP317, AHCYP1, 106 more genes
    nsv7060309inversion1nstd229human GRCh38 chr10: 46,173,677-55,799,586 , GRCh37.p13 chr10: 46,591,857-57,559,346 NPY4R, LOC102724603, 138 more genes
    nsv7060258inversion1nstd229human GRCh38 chr10: 46,241,970-46,840,713 , GRCh37.p13 chr10|NW_003871068.1: 513,085-1,111,828 DUSP8P2, HNRNPA1P33, 23 more genes
    nsv6895769copy number variation1nstd229human GRCh38 chr10: 45,735,504-50,076,220 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 6,619-2,281,126 BMS1P1, AGAP9, 108 more genes
    nsv6886834copy number variation1nstd229human GRCh38 chr10: 45,568,878-51,464,891 , GRCh37.p13 chr10: 46,064,326-53,224,651 PGBD3, MAPK8, 134 more genes
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6878241copy number variation1nstd229human GRCh38 chr10: 46,264,306-46,756,089 , GRCh37.p13 chr10|NW_003871068.1: 535,421-1,027,204 , GRCh37.p13 chr10: 47,023,413-47,746,309 SYT15, LINC00842, 18 more genes
    nsv6637718copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,966,534-51,700,837 , GRCh38.p12 chr10: 45,931,517-49,929,364 CHAT, CTSLP2, 96 more genes
    nsv6637431copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 48,252,675-51,861,565 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 more genes
    nsv6637283copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,269,493-51,874,356 , GRCh38.p12 chr10: 45,774,045-50,114,596 CHAT, CTSLP2, 108 more genes
    nsv6637162copy number variation1nstd102humanUncertain significance GRCh37 chr10: 47,062,985-48,769,625 , GRCh38.p12 chr10: 46,157,935-47,923,579 AHCYP1, SHLD2P3, 51 more genes
    nsv6635765copy number variation3nstd227human GRCh38.p12 chr10: 46,157,935-47,739,149 , GRCh37 chr10: 47,101,942-47,703,869 CTSLP2, GDF2, 48 more genes
    nsv6635526copy number variation2nstd227human GRCh38.p12 chr10: 45,788,238-47,923,579 , GRCh37 chr10: 46,283,686-47,703,869 CTSLP2, GDF2, 65 more genes
    nsv6634784copy number variation1nstd227human GRCh38.p12 chr10: 46,157,935-47,739,149 , GRCh37 chr10: 47,101,942-48,318,619 CTSLP2, GDF2, 48 more genes
    nsv6634443copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,627,470 , GRCh38.p12 chr10: 45,792,373-49,929,364 GLUD1P2, RBP3, 100 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