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 657

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124253insertion1nstd186human GRCh37 chr9: 138,966,309-138,966,349 , GRCh38.p12 chr9: 136,074,463-136,074,503 NACC2
    nsv5961372insertion1nstd209human GRCh38 chr9: 136,023,108-136,023,108 , GRCh37.p13 chr9: 138,914,954-138,914,954 NACC2
    nsv5958862insertion1nstd209human GRCh38 chr9: 136,032,018-136,032,018 , GRCh37.p13 chr9: 138,923,864-138,923,864 NACC2
    nsv5927220copy number variation1nstd209human GRCh38 chr9: 136,045,341-136,045,396 , GRCh37.p13 chr9: 138,937,187-138,937,242 NACC2
    nsv5926645copy number variation1nstd209human GRCh38 chr9: 136,067,641-136,071,348 , GRCh37.p13 chr9: 138,959,487-138,963,194 NACC2
    nsv5924393copy number variation1nstd209human GRCh38 chr9: 136,068,379-136,071,321 , GRCh37.p13 chr9: 138,960,225-138,963,167 NACC2
    nsv5920956copy number variation1nstd209human GRCh38 chr9: 136,007,349-136,007,406 , GRCh37.p13 chr9: 138,899,195-138,899,252 NACC2
    nsv5920621copy number variation1nstd209human GRCh38 chr9: 136,065,336-136,071,260 , GRCh37.p13 chr9: 138,957,182-138,963,106 NACC2
    nsv5919455copy number variation1nstd209human GRCh38 chr9: 136,081,757-136,148,860 , GRCh37.p13 chr9: 138,973,603-139,040,706 NACC2, LOC107987142, 2 more genes
    nsv5918457copy number variation1nstd209human GRCh38 chr9: 136,069,484-136,074,390 , GRCh37.p13 chr9: 138,961,330-138,966,236 NACC2
    nsv5918215copy number variation1nstd209human GRCh38 chr9: 136,045,353-136,045,408 , GRCh37.p13 chr9: 138,937,199-138,937,254 NACC2
    nsv5912641copy number variation1nstd209human GRCh38 chr9: 136,068,309-136,071,353 , GRCh37.p13 chr9: 138,960,155-138,963,199 NACC2
    nsv5910048copy number variation1nstd209human GRCh38 chr9: 136,017,698-136,017,965 , GRCh37.p13 chr9: 138,909,544-138,909,811 NACC2
    nsv5867420copy number variation1nstd209human GRCh38 chr9: 136,070,206-136,074,205 , GRCh37.p13 chr9: 138,962,052-138,966,051 NACC2
    nsv5853925copy number variation2nstd209human GRCh38 chr9: 136,069,166-136,071,405 , GRCh37.p13 chr9: 138,961,012-138,963,251 NACC2
    nsv5852238copy number variation2nstd209human GRCh38 chr9: 136,068,366-136,071,505 , GRCh37.p13 chr9: 138,960,212-138,963,351 NACC2
    nsv5851964copy number variation1nstd209human GRCh38 chr9: 136,090,482-136,092,766 , GRCh37.p13 chr9: 138,982,328-138,984,612 NACC2
    nsv5850722copy number variation1nstd209human GRCh38 chr9: 136,082,056-136,087,481 , GRCh37.p13 chr9: 138,973,902-138,979,327 NACC2
    nsv5850411copy number variation1nstd209human GRCh38 chr9: 136,091,132-136,093,566 , GRCh37.p13 chr9: 138,982,978-138,985,412 NACC2
    nsv5849457copy number variation1nstd209human GRCh38 chr9: 136,095,644-136,101,396 , GRCh37.p13 chr9: 138,987,490-138,993,242 NACC2
    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