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 216

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958273insertion1nstd209human GRCh38 chr6: 99,550,659-99,550,659 , GRCh37.p13 chr6: 99,998,535-99,998,535 TSTD3, CCNC
    nsv5898819copy number variation1nstd209human GRCh38 chr6: 99,556,758-99,557,642 , GRCh37.p13 chr6: 100,004,634-100,005,518 TSTD3, CCNC
    nsv5691674mobile element insertion2nstd211human GRCh38 chr6: 99,550,671-99,550,671 , GRCh37.p13 chr6: 99,998,547-99,998,547 TSTD3, CCNC
    nsv5635558insertion1nstd207human GRCh38 chr6: 99,550,659-99,550,659 , GRCh37.p13 chr6: 99,998,535-99,998,535 CCNC, TSTD3
    nsv5393967mobile element insertion1nstd206human GRCh38 chr6: 99,550,671-99,550,722 , GRCh37.p13 chr6: 99,998,547-99,998,598 CCNC, TSTD3
    nsv5369521translocation1nstd200human GRCh38 chr6: 99,542,723-99,542,723 , GRCh38 chr6: 99,542,864-99,542,864 , GRCh37.p13 chr6: 99,990,599-99,990,599 , GRCh37.p13 chr6: 99,990,740-99,990,740 TSTD3, CCNC
    nsv5363267translocation1nstd200human GRCh38 chr14: 79,684,208-79,684,208 , GRCh38 chr6: 99,542,759-99,542,759 , GRCh37.p13 chr14: 80,150,551-80,150,551 , GRCh37.p13 chr6: 99,990,635-99,990,635 CCNC, NRXN3, 1 more genes
    nsv5338196translocation1nstd200human GRCh37 chr6: 99,990,599-99,990,599 , GRCh37 chr6: 99,990,740-99,990,740 , GRCh38.p12 chr6: 99,542,723-99,542,723 , GRCh38.p12 chr6: 99,542,864-99,542,864 TSTD3, CCNC
    nsv5331727translocation1nstd200human GRCh37 chr6: 99,990,635-99,990,635 , GRCh37 chr14: 80,150,551-80,150,551 , GRCh38.p12 chr14: 79,684,208-79,684,208 , GRCh38.p12 chr6: 99,542,759-99,542,759 CCNC, NRXN3, 1 more genes
    nsv5113063mobile element insertion1nstd203human GRCh38 chr6: 99,550,664-99,550,671 , GRCh37.p13 chr6: 99,998,540-99,998,547 TSTD3, CCNC
    nsv5112246mobile element insertion1nstd203human GRCh38 chr6: 99,550,657-99,550,671 , GRCh37.p13 chr6: 99,998,533-99,998,547 CCNC, TSTD3
    nsv5109647mobile element insertion1nstd203human GRCh38 chr6: 99,550,072-99,550,088 , GRCh37.p13 chr6: 99,997,948-99,997,964 TSTD3, CCNC
    nsv5102841mobile element insertion1nstd203human GRCh38 chr6: 99,550,659-99,550,671 , GRCh37.p13 chr6: 99,998,535-99,998,547 TSTD3, CCNC
    nsv5100967mobile element insertion1nstd203human GRCh38 chr6: 99,550,666-99,550,671 , GRCh37.p13 chr6: 99,998,542-99,998,547 TSTD3, CCNC
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945468copy number variation1nstd200human GRCh38 chr6: 99,537,501-99,540,674 , GRCh37.p13 chr6: 99,985,377-99,988,550 CCNC, TSTD3
    nsv4824577copy number variation1nstd200human GRCh37 chr6: 99,985,377-99,988,550 , GRCh38.p12 chr6: 99,537,501-99,540,674 CCNC, TSTD3
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4725787insertion1nstd186human GRCh37 chr6: 99,998,535-99,998,535 , GRCh38.p12 chr6: 99,550,659-99,550,659 TSTD3, CCNC
    nsv4692302mobile element insertion1nstd186human GRCh37 chr6: 99,998,541-99,998,541 , GRCh38.p12 chr6: 99,550,665-99,550,665 CCNC, TSTD3
    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