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 227

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098082copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,370,797-36,276,941 , GRCh38.p12 chr9: 34,370,799-36,276,944 UNC13B, CD72, 86 more genes
    nsv7098080copy number variation1nstd102humanUncertain significance GRCh37 chr9: 32,453,279-35,068,379 , GRCh38.p12 chr9: 32,453,281-35,068,382 SUGT1P1, RNU7-36P, 110 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv6877458copy number variation1nstd229human GRCh38 chr9: 34,648,944-34,651,240 , GRCh37.p13 chr9: 34,648,941-34,651,237 IL11RA, GALT
    nsv6870133copy number variation1nstd229human GRCh38 chr9: 34,043,094-35,876,103 , GRCh37.p13 chr9: 34,043,092-35,876,100 STOML2, ENHO, 85 more genes
    nsv6868544copy number variation1nstd229human GRCh38 chr9: 34,645,665-34,648,825 , GRCh37.p13 chr9: 34,645,662-34,648,822 GALT
    nsv6868271copy number variation1nstd229human GRCh38 chr9: 34,637,653-34,651,946 , GRCh37.p13 chr9: 34,637,650-34,651,943 SIGMAR1, GALT, 1 more genes
    nsv6864935copy number variation1nstd229human GRCh38 chr9: 34,036,342-35,019,147 , GRCh37.p13 chr9: 34,036,340-35,019,144 SYF2P2, TUBB4BP2, 43 more genes
    nsv6862864copy number variation1nstd229human GRCh38 chr9: 34,646,805-34,646,847 , GRCh37.p13 chr9: 34,646,802-34,646,844 GALT
    nsv6637336copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,247,282-34,986,900 , GRCh38.p12 chr9: 34,247,284-34,986,903 ENHO, SPATA31F1, 29 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
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6451250copy number variation1nstd223human GRCh38 chr9: 34,645,663-34,648,825 , GRCh37.p13 chr9: 34,645,660-34,648,822 GALT
    nsv6449537copy number variation1nstd223human GRCh38 chr9: 34,103,197-34,805,619 , GRCh37.p13 chr9: 34,103,195-34,805,616 LOC105376023, DNAI1, 31 more genes
    nsv6438799copy number variation1nstd223human GRCh38 chr9: 34,648,944-34,651,238 , GRCh37.p13 chr9: 34,648,941-34,651,235 GALT, IL11RA
    nsv6315572copy number variation1nstd102humanUncertain significance GRCh38 chr9: 33,492,358-34,725,916 , GRCh37.p13 chr9: 33,492,356-34,725,913 PTENP1, KIF24, 60 more genes
    nsv6315463copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-35,903,398 , GRCh38.p12 chr9: 203,861-35,903,401 IFNA11P, RNU6-14P, 495 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