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 100

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5531245copy number variation1nstd206human GRCh38 chr19: 6,370,513-6,370,988 , GRCh37.p13 chr19: 6,370,524-6,370,999 CLPP, ALKBH7
    nsv5514137copy number variation1nstd206human GRCh38 chr19: 6,369,271-6,370,336 , GRCh37.p13 chr19: 6,369,282-6,370,347 CLPP
    nsv5285813copy number variation1nstd204human GRCh38.p13 chr19: 5,731,901-6,700,600 , GRCh37.p13 chr19: 5,731,912-6,700,611 MIR6885, LOC390877, 38 more genes
    nsv5027478copy number variation1nstd200human GRCh38 chr19: 6,367,225-6,367,301 , GRCh37.p13 chr19: 6,367,236-6,367,312 CLPP
    nsv5027477copy number variation1nstd200human GRCh38 chr19: 6,358,630-6,389,172 , GRCh37.p13 chr19: 6,358,641-6,389,183 GTF2F1, PSPN, 4 more genes
    nsv4729892copy number variation1nstd102humanUncertain significance GRCh37 chr19: 6,096,399-6,699,729 , GRCh38.p12 chr19: 6,096,388-6,699,718 TUBB4A, KHSRP, 24 more genes
    nsv4676363copy number variation1nstd102humanUncertain significance GRCh37 chr19: 6,246,138-6,823,741 , GRCh38.p12 chr19: 6,246,127-6,823,730 SLC25A23, PSPN, 26 more genes
    nsv4676137copy number variation1nstd102humanUncertain significance GRCh37 chr19: 5,949,772-6,699,729 , GRCh38.p12 chr19: 5,949,761-6,699,718 MIR6885, LOC390877, 27 more genes
    nsv4259986copy number variation1nstd166human GRCh37.p13 chr19: 6,370,394-6,370,999 , GRCh38.p12 chr19: 6,370,383-6,370,988 ALKBH7, CLPP
    nsv3966173insertion1nstd168human GRCh38 chr19: 6,360,305-6,381,599 , GRCh37.p13 chr19: 6,360,316-6,381,610 GTF2F1, PSPN, 3 more genes
    nsv3965657copy number variation1nstd168human GRCh38 chr19: 6,340,790-6,360,305 , GRCh37.p13 chr19: 6,340,801-6,360,316 ACER1, CLPP
    nsv3924480copy number variation1nstd102humanUncertain significance NCBI36 chr19: 5,401,983-6,486,595 , GRCh37.p13 chr19: 5,450,983-6,535,595 , GRCh38.p12 chr19: 5,450,972-6,535,584 TINCR, SAFB2, 42 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923313copy number variation1nstd102humanPathogenic GRCh37 chr19: 4,934,897-6,501,653 , GRCh38 chr19: 4,934,885-6,501,642 , NCBI36 chr19: 4,885,897-6,452,653 LOC105372253, FUT3, 47 more genes
    nsv3918411copy number variation1nstd102humanUncertain significance GRCh38 chr19: 5,905,175-6,916,287 , GRCh37 chr19: 5,905,186-6,916,298 , NCBI36 chr19: 5,856,186-6,867,298 CAPS, MIR6790, 36 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 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