U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 104

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3904672copy number variation1nstd102humanBenign GRCh37 chr9: 15,967,745-16,063,191 , GRCh38.p12 chr9: 15,967,747-16,063,193 CCDC171
    nsv3909786copy number variation1nstd102humanBenign GRCh37 chr9: 16,009,322-16,033,109 , GRCh38.p12 chr9: 16,009,324-16,033,111 CCDC171
    nsv6638026copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,823,399-15,947,615 , GRCh38.p12 chr9: 15,823,401-15,947,617 CCDC171
    nsv4676078copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,901,665-15,994,736 , GRCh38.p12 chr9: 15,901,667-15,994,738 CCDC171
    nsv3915680copy number variation1nstd102humanUncertain significance NCBI36 chr9: 15,653,456-15,886,775 , GRCh37.p13 chr9: 15,663,456-15,896,775 , GRCh38.p12 chr9: 15,663,458-15,896,777 CCDC171, LOC107987049, 1 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 CCDC171, RPL4P5, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 CCDC171, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 CCDC171, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 CCDC171, DOCK8-AS1, 186 more genes
    nsv3910119copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357 CCDC171, RNA5SP279, 186 more genes
    nsv3917303copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357 CCDC171, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 CCDC171, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 CCDC171, RANBP6, 184 more genes
    nsv3899178copy number variation1nstd102humanPathogenic GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752 CCDC171, GLIS3, 181 more genes
    nsv3903505copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895 CCDC171, RPS26P3, 179 more genes
    nsv3923785copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-16,887,578 , GRCh37 chr9: 204,193-16,897,578 , GRCh38 chr9: 204,193-16,897,580 CCDC171, FTH1P12, 176 more genes
    nsv3890932copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-16,856,907 , GRCh38.p12 chr9: 203,861-16,856,909 CCDC171, ACTG1P14, 176 more genes
    nsv3917732copy number variation1nstd102humanPathogenic GRCh38 chr9: 214,367-16,307,944 , GRCh37 chr9: 214,367-16,307,942 , NCBI36 chr9: 204,367-16,297,942 CCDC171, RLN1, 173 more genes
    nsv3919683copy number variation1nstd102humanPathogenic GRCh38 chr9: 322,690-16,401,656 , NCBI36 chr9: 312,690-16,391,654 , GRCh37 chr9: 322,690-16,401,654 CCDC171, DMRT2, 172 more genes
    nsv6315395copy number variation1nstd102humanPathogenic GRCh37 chr9: 4,992,582-19,322,101 , GRCh38.p12 chr9: 4,992,582-19,322,103 CCDC171, FREM1, 142 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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