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 192

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7051399inversion1nstd229human GRCh38 chr6: 166,288,025-166,326,733 , GRCh37.p13 chr6: 166,701,513-166,740,221 LOC107986669, SFT2D1, 1 more genes
    nsv7039011inversion1nstd229human GRCh38 chr6: 163,643,496-167,786,105 , GRCh37.p13 chr6: 164,064,528-168,186,785 HNRNPA1P49, CCR6, 70 more genes
    nsv6816043copy number variation1nstd229human GRCh38 chr6: 165,919,144-166,571,192 , GRCh37.p13 chr6: 166,332,632-166,984,680 HNRNPA1P49, MIR1913, 19 more genes
    nsv6814470copy number variation1nstd229human GRCh38 chr6: 166,306,033-166,306,689 , GRCh37.p13 chr6: 166,719,521-166,720,177 LOC107986669, PRR18
    nsv6807032copy number variation1nstd229human GRCh38 chr6: 166,264,628-166,373,652 , GRCh37.p13 chr6: 166,678,116-166,787,140 LOC105378118, SFT2D1, 5 more genes
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
    nsv6634373copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581 LOC107986547, LOC107986550, 132 more genes
    nsv6619337copy number variation1nstd223human GRCh38 chr6: 166,304,477-166,304,659 , GRCh37.p13 chr6: 166,717,965-166,718,147 PRR18
    nsv6556844inversion1nstd223human GRCh38 chr6: 161,649,493-166,382,472 , GRCh37.p13 chr6: 162,070,525-166,795,960 RNU6-730P, TRE-TTC15-1, 49 more genes
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6313793copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,212,864-170,919,482 , GRCh38.p12 chr6: 161,791,832-170,610,394 LOC645468, GPR31, 148 more genes
    nsv6313745copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,290,087-170,919,482 , GRCh38.p12 chr6: 162,869,055-170,610,394 HGC6.3, LOC112267970, 143 more genes
    nsv6313560copy number variation1nstd102humanPathogenic GRCh37 chr6: 161,047,873-170,919,482 , GRCh38.p12 chr6: 160,626,841-170,610,394 LOC105378142, LOC100289495, 159 more genes
    nsv5917264copy number variation1nstd209human GRCh38 chr6: 166,304,477-166,304,658 , GRCh37.p13 chr6: 166,717,965-166,718,146 PRR18
    nsv5455143copy number variation1nstd206human GRCh38 chr6: 166,304,479-166,304,659 , GRCh37.p13 chr6: 166,717,967-166,718,147 PRR18
    nsv5363541translocation1nstd200human GRCh38 chr6: 166,307,858-166,307,858 , GRCh38 chr6: 166,307,976-166,307,976 , GRCh37.p13 chr6: 166,721,346-166,721,346 , GRCh37.p13 chr6: 166,721,464-166,721,464 LOC107986669, PRR18
    nsv5331622translocation1nstd200human GRCh37 chr6: 166,718,147-166,718,147 , GRCh37 chr6: 166,717,967-166,717,967 , GRCh38.p12 chr6: 166,304,659-166,304,659 , GRCh38.p12 chr6: 166,304,479-166,304,479 PRR18
    nsv4968655copy number variation1nstd200human GRCh38 chr6: 165,587,706-166,398,601 , GRCh37.p13 chr6: 166,001,194-166,812,089 LOC105378115, TBXT, 19 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