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 336

    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
    nsv7050776inversion1nstd229human GRCh38 chr7: 1,736,445-2,580,576 , GRCh37.p13 chr7: 1,776,081-2,620,210 IMMP1LP3, GRIFIN, 21 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
    nsv6816810copy number variation1nstd229human GRCh38 chr7: 2,405,005-2,412,014 , GRCh37.p13 chr7: 2,444,640-2,451,649 CHST12
    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
    nsv6813907copy number variation1nstd229human GRCh38 chr7: 2,430,623-2,441,793 , GRCh37.p13 chr7: 2,470,258-2,481,428 CHST12
    nsv6813550copy number variation1nstd229human GRCh38 chr7: 2,423,758-2,424,397 , GRCh37.p13 chr7: 2,463,393-2,464,032 CHST12
    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
    nsv6810174copy number variation1nstd229human GRCh38 chr7: 2,434,658-2,441,555 , GRCh37.p13 chr7: 2,474,293-2,481,190 CHST12
    nsv6809478copy number variation1nstd229human GRCh38 chr7: 2,415,649-2,419,276 , GRCh37.p13 chr7: 2,455,284-2,458,911 CHST12
    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
    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
    nsv6803024copy number variation1nstd229human GRCh38 chr7: 2,160,119-2,450,631 , GRCh37.p13 chr7: 2,199,754-2,490,266 MIR6836, SNX8, 9 more genes
    nsv6800320copy number variation1nstd229human GRCh38 chr7: 2,398,427-2,439,690 , GRCh37.p13 chr7: 2,438,062-2,479,325 CHST12
    nsv6799373copy number variation1nstd229human GRCh38 chr7: 2,398,203-2,401,834 , GRCh37.p13 chr7: 2,437,838-2,441,469 CHST12
    nsv6799019copy number variation1nstd229human GRCh38 chr7: 2,440,066-2,458,062 , GRCh37.p13 chr7: 2,479,701-2,497,697 CHST12
    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