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 236

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057791inversion1nstd229human GRCh38 chr7: 23,513,468-23,515,326 , GRCh37.p13 chr7: 23,553,087-23,554,945 TRA2A
    nsv7057183inversion1nstd229human GRCh38 chr7: 21,972,222-23,503,741 , GRCh37.p13 chr7: 22,011,840-23,543,360 TRA2A, IGF2BP3, 30 more genes
    nsv7049867inversion1nstd229human GRCh38 chr7: 23,516,897-26,099,511 , GRCh37.p13 chr7: 23,556,516-26,139,131 NPY, LINC03007, 34 more genes
    nsv7042193inversion1nstd229human GRCh38 chr7: 23,162,006-23,606,884 , GRCh37.p13 chr7: 23,201,625-23,646,503 NUP42, RPS2P32, 13 more genes
    nsv7042130inversion1nstd229human GRCh38 chr7: 23,500,611-26,098,164 , GRCh37.p13 chr7: 23,540,230-26,137,784 CLK2P1, RNA5SP228, 34 more genes
    nsv6816855copy number variation1nstd229human GRCh38 chr7: 23,264,438-23,888,561 , GRCh37.p13 chr7: 23,304,057-23,928,180 RNU7-143P, FCF1P1, 15 more genes
    nsv6812556copy number variation1nstd229human GRCh38 chr7: 23,333,514-23,568,866 , GRCh37.p13 chr7: 23,373,133-23,608,485 LOC442517, RPS2P32, 5 more genes
    nsv6808186copy number variation1nstd229human GRCh38 chr7: 23,510,587-23,522,038 , GRCh37.p13 chr7: 23,550,206-23,561,657 TRA2A
    nsv6806128copy number variation1nstd229human GRCh38 chr7: 23,518,683-23,521,778 , GRCh37.p13 chr7: 23,558,302-23,561,397 TRA2A
    nsv6805800copy number variation1nstd229human GRCh38 chr7: 23,509,585-23,509,673 , GRCh37.p13 chr7: 23,549,204-23,549,292 TRA2A
    nsv6804292copy number variation1nstd229human GRCh38 chr7: 23,510,475-23,518,621 , GRCh37.p13 chr7: 23,550,094-23,558,240 TRA2A
    nsv6803152copy number variation1nstd229human GRCh38 chr7: 23,503,701-23,606,900 , GRCh37.p13 chr7: 23,543,320-23,646,519 LOC442517, CCDC126, 3 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6604620copy number variation1nstd223human GRCh38 chr7: 23,496,556-23,536,939 , GRCh37.p13 chr7: 23,536,175-23,576,558 TRA2A
    nsv6570951inversion1nstd223human GRCh38 chr7: 23,517,219-23,518,580 , GRCh37.p13 chr7: 23,556,838-23,558,199 TRA2A
    nsv6566268inversion1nstd223human GRCh38 chr7: 23,520,265-23,520,380 , GRCh37.p13 chr7: 23,559,884-23,559,999 TRA2A
    nsv6561581inversion1nstd223human GRCh38 chr7: 23,508,587-23,509,544 , GRCh37.p13 chr7: 23,548,206-23,549,163 TRA2A
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6261183mobile element insertion1nstd215human GRCh38 chr7: 23,522,568-23,522,568 , GRCh37.p13 chr7: 23,562,187-23,562,187 TRA2A
    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