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 110

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074499inversion1nstd229human GRCh38 chr10: 6,256,776-7,627,290 , GRCh37.p13 chr10: 6,298,739-7,669,253 LOC105376387, COX6CP17, 20 more genes
    nsv7070626inversion1nstd229human GRCh38 chr10: 2,965,996-7,388,650 , GRCh37.p13 chr10: 3,008,188-7,430,612 AKR1E2, LOC105376360, 100 more genes
    nsv7058770inversion1nstd229human GRCh38 chr10: 2,888,994-6,942,658 , GRCh37.p13 chr10: 2,931,186-6,984,620 LOC105376358, LOC105376381, 96 more genes
    nsv7058192inversion1nstd229human GRCh38 chr10: 6,343,456-7,164,858 , GRCh37.p13 chr10: 6,385,418-7,206,820 LINP1, LOC107984203, 10 more genes
    nsv6891451copy number variation1nstd229human GRCh38 chr10: 6,581,994-6,587,599 , GRCh37.p13 chr10: 6,623,956-6,629,561 PRKCQ-AS1
    nsv6891429copy number variation1nstd229human GRCh38 chr10: 3,284,212-7,401,139 , GRCh37.p13 chr10: 3,326,404-7,443,101 LOC105376358, MIR3155B, 91 more genes
    nsv6885503copy number variation1nstd229human GRCh38 chr10: 6,538,201-6,589,200 , GRCh37.p13 chr10: 6,580,163-6,631,162 PRKCQ-AS1, PRKCQ
    nsv6637939copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,027-12,648,149 , GRCh38.p12 chr10: 54,087-12,606,150 LARP4B-DT, CALML5, 206 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6290853copy number variation1nstd102humanUncertain significance GRCh37 chr10: 4,927,427-6,653,936 , GRCh38.p12 chr10: 4,885,235-6,611,974 AKR1C4, FBH1, 51 more genes
    nsv6131797copy number variation1nstd213human GRCh37 chr10: 6,580,000-6,710,001 , GRCh38.p12 chr10: 6,538,038-6,668,039 PRKCQ, PRKCQ-AS1, 1 more genes
    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
    nsv4612624copy number variation1nstd183human GRCh37 chr10: 6,622,134-6,622,179 , GRCh38.p12 chr10: 6,580,172-6,580,217 PRKCQ-AS1, PRKCQ
    nsv4607099copy number variation1nstd183human GRCh37 chr10: 6,496,104-6,706,872 , GRCh38.p12 chr10: 6,454,142-6,664,910 LINC02648, PRKCQ, 2 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
    nsv4183698copy number variation1nstd166human GRCh37.p13 chr10: 6,618,688-6,620,544 , GRCh38.p12 chr10: 6,576,726-6,578,582 PRKCQ-AS1, PRKCQ
    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
    nsv3923991copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 1,633,367-9,285,698 , GRCh37 chr10: 1,643,367-9,245,692 , GRCh38 chr10: 1,601,172-9,203,729 ADARB2, ATP5F1C, 143 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