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 74

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5926346copy number variation1nstd209human GRCh38 chr10: 116,907,211-116,907,272 , GRCh37.p13 chr10: 118,666,722-118,666,783 ENO4, SHTN1
    nsv5912687copy number variation1nstd209human GRCh38 chr10: 116,904,904-116,905,223 , GRCh37.p13 chr10: 118,664,415-118,664,734 ENO4, SHTN1
    nsv5695174mobile element insertion1nstd211human GRCh38 chr10: 116,891,226-116,891,226 , GRCh37.p13 chr10: 118,650,737-118,650,737 SHTN1, ENO4
    nsv5504691copy number variation1nstd206human GRCh38 chr10: 116,904,919-116,905,224 , GRCh37.p13 chr10: 118,664,430-118,664,735 SHTN1, ENO4
    nsv5498140copy number variation1nstd206human GRCh38 chr10: 116,893,693-116,894,984 , GRCh37.p13 chr10: 118,653,204-118,654,495 SHTN1, ENO4
    nsv5496827copy number variation1nstd206human GRCh38 chr10: 116,901,114-116,901,164 , GRCh37.p13 chr10: 118,660,625-118,660,675 SHTN1, ENO4
    nsv5413100mobile element insertion1nstd206human GRCh38 chr10: 116,891,226-116,891,277 , GRCh37.p13 chr10: 118,650,737-118,650,788 SHTN1, ENO4
    nsv5207407mobile element deletion1nstd204human GRCh37.p13 chr10: 118,664,407-118,664,756 , GRCh38.p13 chr10: 116,904,896-116,905,245 SHTN1, ENO4
    nsv5127282mobile element insertion1nstd203human GRCh38 chr10: 116,882,377-116,882,391 , GRCh37.p13 chr10: 118,641,888-118,641,902 ENO4, SHTN1
    nsv4977110copy number variation1nstd200human GRCh38 chr10: 116,861,937-116,863,482 , GRCh37.p13 chr10: 118,621,448-118,622,993 ENO4
    nsv4974084copy number variation1nstd200human GRCh38 chr10: 116,595,727-116,900,521 , GRCh37.p13 chr10|NW_003871069.1: 6,723-196,262 , GRCh37.p13 chr10: 118,355,239-118,544,777 HSPA12A, SPMIP5, 8 more genes
    nsv4899595mobile element deletion1nstd200human GRCh38 chr10: 116,904,919-116,905,224 , GRCh37.p13 chr10: 118,664,430-118,664,735 ENO4, SHTN1
    nsv4841657copy number variation1nstd200human GRCh37 chr10: 118,355,239-118,660,032 , GRCh38.p12 chr10: 116,595,727-116,900,521 HSPA12A-AS1, PNLIPRP2, 8 more genes
    nsv4774848mobile element deletion1nstd200human GRCh37 chr10: 118,664,430-118,664,735 , GRCh38.p12 chr10: 116,904,919-116,905,224 SHTN1, ENO4
    nsv4617026copy number variation1nstd183human GRCh37 chr10: 118,624,015-118,624,074 , GRCh38.p12 chr10: 116,864,504-116,864,563 ENO4
    nsv4571745mobile element insertion1nstd166human GRCh37.p13 chr10: 118,643,409-118,643,409 , GRCh38.p12 chr10: 116,883,898-116,883,898 ENO4, SHTN1
    nsv4528038copy number variation1nstd166human GRCh37.p13 chr10: 118,613,835-118,614,545 , GRCh38.p12 chr10: 116,854,324-116,855,034 ENO4
    nsv4489233mobile element insertion1nstd166human GRCh37.p13 chr10: 118,635,322-118,635,322 , GRCh38.p12 chr10: 116,875,811-116,875,811 ENO4
    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