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 429

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098914copy number variation1nstd102humanUncertain significance GRCh38 chr9: 68,417,620-68,744,894 , GRCh37.p13 chr9: 71,130,848-71,359,810 PGM5, TMEM252-DT, 5 more genes
    nsv7064084inversion1nstd229human GRCh38 chr9: 64,120,773-68,530,496 , GRCh37.p13 chr9: 40,041,911-44,672,613 LOC112267859, ZNG1C, 91 more genes
    nsv7063651inversion1nstd229human GRCh38 chr9: 68,439,628-68,439,761 , GRCh37.p13 chr9|NW_003871067.1: 219,076-219,209 , GRCh37.p13 chr9: 71,054,544-71,054,677 PGM5
    nsv6877274copy number variation1nstd229human GRCh38 chr9: 68,484,957-68,489,541 , GRCh37.p13 chr9|NW_003871067.1: 264,405-268,989 , GRCh37.p13 chr9: 71,099,873-71,104,457 PGM5
    nsv6877087copy number variation1nstd229human GRCh38 chr9: 68,477,454-68,477,637 , GRCh37.p13 chr9|NW_003871067.1: 256,902-257,085 , GRCh37.p13 chr9: 71,092,370-71,092,553 PGM5
    nsv6870603copy number variation1nstd229human GRCh38 chr9: 68,444,616-68,444,642 , GRCh37.p13 chr9|NW_003871067.1: 224,064-224,090 , GRCh37.p13 chr9: 71,059,532-71,059,558 PGM5
    nsv6867351copy number variation1nstd229human GRCh38 chr9: 68,330,601-68,445,300 , GRCh37.p13 chr9|NW_003871067.1: 110,049-224,748 , GRCh37.p13 chr9: 70,945,517-71,060,216 PGM5, LOC101929800, 3 more genes
    nsv6866080copy number variation1nstd229human GRCh38 chr9: 68,411,408-68,411,445 , GRCh37.p13 chr9: 71,026,324-71,026,361 , GRCh37.p13 chr9|NW_003871067.1: 190,856-190,893 PGM5
    nsv6864014copy number variation1nstd229human GRCh38 chr9: 68,499,362-68,529,563 , GRCh37.p13 chr9|NW_003871067.1: 278,810-295,379 , GRCh37.p13 chr9: 71,114,278-71,130,847 PGM5
    nsv6862625copy number variation1nstd229human GRCh38 chr9: 68,450,661-68,451,652 , GRCh37.p13 chr9: 71,065,577-71,066,568 , GRCh37.p13 chr9|NW_003871067.1: 230,109-231,100 PGM5
    nsv6860832copy number variation1nstd229human GRCh38 chr9: 68,452,278-68,452,474 , GRCh37.p13 chr9|NW_003871067.1: 231,726-231,922 , GRCh37.p13 chr9: 71,067,194-71,067,390 PGM5
    nsv6860589copy number variation1nstd229human GRCh38 chr9: 68,516,303-68,525,125 , GRCh37.p13 chr9: 71,131,219-71,140,041 PGM5
    nsv6860418copy number variation1nstd229human GRCh38 chr9: 68,502,328-68,502,434 , GRCh37.p13 chr9|NW_003871067.1: 281,776-281,882 , GRCh37.p13 chr9: 71,117,244-71,117,350 PGM5
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633472copy number variation1nstd224human GRCh37 chr9: 70,990,841-71,020,205 , GRCh38.p12 chr9: 68,375,925-68,405,289 PGM5, LOC105376070
    nsv6573474inversion1nstd223human GRCh38 chr9: 68,432,341-68,434,246 , GRCh37.p13 chr9|NW_003871067.1: 211,789-213,694 , GRCh37.p13 chr9: 71,047,257-71,049,162 PGM5
    nsv6454489copy number variation1nstd223human GRCh38 chr9: 68,516,303-68,525,121 , GRCh37.p13 chr9: 71,131,219-71,140,037 PGM5
    nsv6454433copy number variation1nstd223human GRCh38 chr9: 68,426,964-68,446,526 , GRCh37.p13 chr9|NW_003871067.1: 206,412-225,974 , GRCh37.p13 chr9: 71,041,880-71,061,442 PGM5
    nsv6453214copy number variation1nstd223human GRCh38 chr9: 68,456,203-68,460,136 , GRCh37.p13 chr9|NW_003871067.1: 235,651-239,584 , GRCh37.p13 chr9: 71,071,119-71,075,052 PGM5
    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