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 242

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925687copy number variation1nstd209human GRCh38 chr9: 135,623,539-135,623,598 , GRCh37.p13 chr9: 138,515,385-138,515,444 GLT6D1
    nsv5626869insertion1nstd207human GRCh38 chr9: 135,623,572-135,623,572 , GRCh37.p13 chr9: 138,515,418-138,515,418 GLT6D1
    nsv5489036copy number variation1nstd206human GRCh38 chr9: 135,634,724-135,634,809 , GRCh37.p13 chr9: 138,526,570-138,526,655 GLT6D1
    nsv5479745copy number variation1nstd206human GRCh38 chr9: 135,641,460-135,642,171 , GRCh37.p13 chr9: 138,533,306-138,534,017 GLT6D1
    nsv4973320copy number variation1nstd200human GRCh38 chr9: 135,619,689-135,622,411 , GRCh37.p13 chr9: 138,511,535-138,514,257 LOC102723971, GLT6D1
    nsv4755644insertion1nstd199human GRCh37 chr9: 138,515,402-138,515,402 , GRCh38.p12 chr9: 135,623,556-135,623,556 GLT6D1
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4684240copy number variation1nstd102humanUncertain significance GRCh37 chr9: 137,880,493-138,781,516 , GRCh38.p12 chr9: 134,988,647-135,889,670 LINC01502, LOC107987040, 25 more genes
    nsv4647940copy number variation1nstd186human GRCh37 chr9: 138,515,385-138,515,447 , GRCh38.p12 chr9: 135,623,539-135,623,601 GLT6D1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4453311copy number variation1nstd102humanUncertain significance GRCh37 chr9: 134,379,574-138,678,377 , GRCh38.p12 chr9: 131,504,187-135,786,531 RNU6ATAC, RPL21P81, 114 more genes
    nsv4185310copy number variation1nstd166human GRCh37.p13 chr9: 138,516,448-138,519,192 , GRCh38.p12 chr9: 135,624,602-135,627,346 GLT6D1
    nsv4184425copy number variation1nstd166human GRCh37.p13 chr9: 138,515,385-138,515,447 , GRCh38.p12 chr9: 135,623,539-135,623,601 GLT6D1
    nsv4175296copy number variation1nstd166human GRCh37.p13 chr9: 138,522,575-138,522,631 , GRCh38.p12 chr9: 135,630,729-135,630,785 GLT6D1
    nsv3924922copy number variation1nstd102humanPathogenic GRCh38 chr9: 133,504,071-138,159,073 , NCBI36 chr9: 135,314,179-140,173,346 , GRCh37 chr9: 136,324,358-141,053,525 SETP5, NRARP, 178 more genes
    nsv3923661copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,056,830-139,331,499 , NCBI36 chr9: 137,196,651-138,451,320 , GRCh38 chr9: 135,164,984-136,437,047 CAMSAP1, NACC2, 41 more genes
    nsv3922926copy number variation1nstd102humanPathogenic NCBI36 chr9: 137,483,683-139,628,011 , GRCh37 chr9: 138,343,862-140,508,190 , GRCh38 chr9: 135,452,016-137,613,738 SSNA1, LOC107987140, 126 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 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