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 321

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057091inversion1nstd229human GRCh38 chr7: 2,273,784-2,696,327 , GRCh37.p13 chr7: 2,313,419-2,735,961 BRAT1, NGRNP3, 13 more genes
    nsv7053928inversion1nstd229human GRCh38 chr7: 1,791,275-2,573,914 , GRCh37.p13 chr7: 1,830,911-2,613,548 MIR4655, LOC105375127, 19 more genes
    nsv7052786inversion1nstd229human GRCh38 chr7: 2,451,109-6,490,439 , GRCh37.p13 chr7: 2,490,744-6,530,070 LOC105375130, DAGLB, 72 more genes
    nsv7050776inversion1nstd229human GRCh38 chr7: 1,736,445-2,580,576 , GRCh37.p13 chr7: 1,776,081-2,620,210 IMMP1LP3, GRIFIN, 21 more genes
    nsv7048338inversion1nstd229human GRCh38 chr7: 2,508,497-2,570,079 , GRCh37.p13 chr7: 2,548,131-2,609,713 LFNG, MIR4648, 3 more genes
    nsv7042414inversion1nstd229human GRCh38 chr7: 2,257,030-2,573,543 , GRCh37.p13 chr7: 2,296,665-2,613,177 LOC107986759, GRIFIN, 11 more genes
    nsv7041506inversion1nstd229human GRCh38 chr7: 1,807,124-2,573,544 , GRCh37.p13 chr7: 1,846,760-2,613,178 CHST12, LOC100127955, 19 more genes
    nsv6817590copy number variation1nstd229human GRCh38 chr7: 2,434,605-2,553,455 , GRCh37.p13 chr7: 2,474,240-2,593,089 LOC107986759, LFNG, 4 more genes
    nsv6817445copy number variation1nstd229human GRCh38 chr7: 2,514,730-2,515,222 , GRCh37.p13 chr7: 2,554,364-2,554,856 LFNG
    nsv6817401copy number variation1nstd229human GRCh38 chr7: 2,492,201-2,559,500 , GRCh37.p13 chr7: 2,531,835-2,599,134 BRAT1, MIR4648, 3 more genes
    nsv6816771copy number variation1nstd229human GRCh38 chr7: 2,514,401-2,539,400 , GRCh37.p13 chr7: 2,554,035-2,579,034 MIR4648, LFNG, 1 more genes
    nsv6815704copy number variation1nstd229human GRCh38 chr7: 2,256,868-2,660,330 , GRCh37.p13 chr7: 2,296,503-2,699,964 NGRNP3, IMMP1LP3, 13 more genes
    nsv6811734copy number variation1nstd229human GRCh38 chr7: 2,099,185-2,523,523 , GRCh37.p13 chr7: 2,138,820-2,563,157 CHST12, NUDT1, 13 more genes
    nsv6808763copy number variation1nstd229human GRCh38 chr7: 2,361,837-2,647,130 , GRCh37.p13 chr7: 2,401,472-2,686,764 KIF19BP, TTYH3, 10 more genes
    nsv6808276copy number variation1nstd229human GRCh38 chr7: 2,512,980-2,575,679 , GRCh37.p13 chr7: 2,552,614-2,615,313 MIR4648, BRAT1, 2 more genes
    nsv6808003copy number variation1nstd229human GRCh38 chr7: 2,518,501-2,519,900 , GRCh37.p13 chr7: 2,558,135-2,559,534 LFNG
    nsv6804638copy number variation1nstd229human GRCh38 chr7: 2,359,001-2,521,600 , GRCh37.p13 chr7: 2,398,636-2,561,234 NGRNP3, GRIFIN, 5 more genes
    nsv6804498copy number variation1nstd229human GRCh38 chr7: 2,418,672-2,518,226 , GRCh37.p13 chr7: 2,458,307-2,557,860 LFNG, LOC107986759, 2 more genes
    nsv6801253copy number variation1nstd229human GRCh38 chr7: 2,526,139-2,540,164 , GRCh37.p13 chr7: 2,565,773-2,579,798 MIR4648, BRAT1, 1 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 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