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 144

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925717copy number variation1nstd209human GRCh38 chr10: 4,654,489-4,655,149 , GRCh37.p13 chr10: 4,696,681-4,697,341 LINC00705, MANCR
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PITRM1-AS1, TRV-TAC3-1, 133 more genes
    nsv5480819copy number variation1nstd206human GRCh38 chr10: 4,654,783-4,654,908 , GRCh37.p13 chr10: 4,696,975-4,697,100 MANCR, LINC00705
    nsv4986123copy number variation1nstd200human GRCh38 chr10: 4,660,197-4,660,992 , GRCh37.p13 chr10: 4,702,389-4,703,184 MANCR, LINC00705
    nsv4986122copy number variation1nstd200human GRCh38 chr10: 4,656,568-4,657,966 , GRCh37.p13 chr10: 4,698,760-4,700,158 LINC00705, MANCR
    nsv4986121copy number variation1nstd200human GRCh38 chr10: 4,654,783-4,654,908 , GRCh37.p13 chr10: 4,696,975-4,697,100 MANCR, LINC00705
    nsv4849193copy number variation1nstd200human GRCh37 chr10: 4,702,389-4,703,184 , GRCh38.p12 chr10: 4,660,197-4,660,992 MANCR, LINC00705
    nsv4839906copy number variation1nstd200human GRCh37 chr10: 4,698,760-4,700,158 , GRCh38.p12 chr10: 4,656,568-4,657,966 LINC00705, MANCR
    nsv4675705copy number variation1nstd102humanUncertain significance GRCh37 chr10: 4,652,848-4,893,519 , GRCh38.p12 chr10: 4,610,656-4,851,327 LOC107984197, LOC105376374, 5 more genes
    nsv4674854copy number variation1nstd102humanLikely benign GRCh37 chr10: 4,504,067-5,395,279 , GRCh38.p12 chr10: 4,461,875-5,353,316 AKR1C8, LINC02561, 18 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4421196copy number variation1nstd174human GRCh37 chr10: 4,700,968-4,711,764 , GRCh38.p12 chr10: 4,658,776-4,669,572 MANCR, LINC00705, 1 more genes
    nsv4188525copy number variation1nstd166human GRCh37.p13 chr10: 3,717,335-4,859,752 , GRCh38.p12 chr10: 3,675,143-4,817,560 , LINC00703, 24 more genes
    nsv4186337copy number variation1nstd166human GRCh37.p13 chr10: 4,696,975-4,697,100 , GRCh38.p12 chr10: 4,654,783-4,654,908 LINC00705, MANCR
    nsv4179146copy number variation1nstd166human GRCh37.p13 chr10: 4,702,389-4,703,184 , GRCh38.p12 chr10: 4,660,197-4,660,992 MANCR, LINC00705
    nsv4177773copy number variation1nstd166human GRCh37.p13 chr10: 4,696,685-4,697,342 , GRCh38.p12 chr10: 4,654,493-4,655,150 LINC00705, MANCR
    nsv3961849copy number variation1nstd168human GRCh38 chr10: 4,631,418-4,713,681 , GRCh37.p13 chr10: 4,673,610-4,755,873 LOC105376373, MANCR, 3 more genes
    nsv3924674copy number variation1nstd102humanUncertain significance NCBI36 chr10: 4,354,730-5,034,952 , GRCh37.p13 chr10: 4,364,730-5,044,952 , GRCh38.p12 chr10: 4,322,538-5,002,760 LOC107984197, LOC105376374, 14 more genes
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
    nsv3924330copy number variation1nstd102humanUncertain significance GRCh38 chr10: 4,605,831-7,403,265 , GRCh37 chr10: 4,648,023-7,445,227 , NCBI36 chr10: 4,638,023-7,485,233 AKR1C8, LINC02649, 67 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