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 35

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3914771copy number variation1nstd102humanPathogenic GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909 PRKCQ, COX6CP17, 302 more genes
    nsv3884983copy number variation1nstd102humanPathogenic GRCh37 chr10: 4,689,760-19,120,882 , GRCh38.p12 chr10: 4,647,568-18,831,953 PRKCQ, HSPA14, 228 more genes
    nsv3918372copy number variation1nstd102humanPathogenic GRCh38 chr10: 70,478-13,736,564 , GRCh37 chr10: 224,406-13,778,564 , NCBI36 chr10: 106,418-13,818,570 PRKCQ, IL9RP2, 232 more genes
    nsv3890577copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-12,842,179 , GRCh38.p12 chr10: 54,086-12,800,180 PRKCQ, LOC105376364, 208 more genes
    nsv3911206copy number variation1nstd102humanPathogenic GRCh37 chr10: 4,844,945-16,865,490 , NCBI36 chr10: 4,834,945-16,905,496 , GRCh38 chr10: 4,802,753-16,823,491 PRKCQ, LINC02656, 200 more genes
    nsv3893746copy number variation1nstd102humanPathogenic GRCh37 chr10: 136,361-8,850,609 , GRCh38.p12 chr10: 90,421-8,808,646 PRKCQ, TRV-TAC3-1, 163 more genes
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PRKCQ, PITRM1-AS1, 133 more genes
    nsv3907813copy number variation1nstd102humanPathogenic GRCh37 chr10: 2,593,113-8,484,746 , GRCh38.p12 chr10: 2,550,921-8,442,783 PRKCQ, AKR1C6P, 121 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 PRKCQ, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 PRKCQ, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 PRKCQ, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 PRKCQ, TUBB8, 2085 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 PRKCQ, LINC00700, 806 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 PRKCQ, EPC1-AS1, 559 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 PRKCQ, RPL36AP55, 418 more genes
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 PRKCQ, RN7SKP241, 389 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 PRKCQ, WDR37, 302 more genes
    nsv3920285copy number variation1nstd102humanPathogenic NCBI36 chr10: 106,418-15,455,341 , GRCh37.p13 chr10: 116,418-15,415,335 , GRCh38.p12 chr10: 70,478-15,373,336 PRKCQ, NRBF2P5, 265 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 PRKCQ, LOC105376357, 264 more genes
    nsv3915964copy number variation1nstd102humanPathogenic NCBI36 chr10: 90,026-13,287,922 , GRCh38 chr10: 54,086-13,205,916 , GRCh37 chr10: 100,026-13,247,916 PRKCQ, LOC105376409, 217 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