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 1054

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974958inversion1nstd209human GRCh38 chr9: 17,189,530-17,712,557 , GRCh37.p13 chr9: 17,189,528-17,712,555 SH3GL2, CNTLN, 3 more genes
    nsv5967504insertion1nstd209human GRCh38 chr9: 17,312,364-17,312,364 , GRCh37.p13 chr9: 17,312,362-17,312,362 CNTLN
    nsv5956729insertion1nstd209human GRCh38 chr9: 17,274,304-17,274,304 , GRCh37.p13 chr9: 17,274,302-17,274,302 CNTLN
    nsv5923640copy number variation1nstd209human GRCh38 chr9: 17,257,497-17,263,480 , GRCh37.p13 chr9: 17,257,495-17,263,478 CNTLN
    nsv5923184copy number variation1nstd209human GRCh38 chr9: 17,277,059-17,277,284 , GRCh37.p13 chr9: 17,277,057-17,277,282 CNTLN
    nsv5922936copy number variation1nstd209human GRCh38 chr9: 17,178,946-17,179,264 , GRCh37.p13 chr9: 17,178,944-17,179,262 CNTLN
    nsv5920740copy number variation1nstd209human GRCh38 chr9: 17,401,464-17,406,984 , GRCh37.p13 chr9: 17,401,462-17,406,982 CNTLN
    nsv5920514copy number variation1nstd209human GRCh38 chr9: 17,346,274-17,346,342 , GRCh37.p13 chr9: 17,346,272-17,346,340 CNTLN
    nsv5920348copy number variation1nstd209human GRCh38 chr9: 17,415,240-17,415,354 , GRCh37.p13 chr9: 17,415,238-17,415,352 CNTLN
    nsv5918377copy number variation1nstd209human GRCh38 chr9: 17,144,798-17,145,139 , GRCh37.p13 chr9: 17,144,796-17,145,137 CNTLN
    nsv5913955copy number variation1nstd209human GRCh38 chr9: 17,183,042-17,183,106 , GRCh37.p13 chr9: 17,183,040-17,183,104 CNTLN
    nsv5913576copy number variation1nstd209human GRCh38 chr9: 17,441,721-17,446,686 , GRCh37.p13 chr9: 17,441,719-17,446,684 CNTLN, SAMM50P1
    nsv5912860copy number variation1nstd209human GRCh38 chr9: 17,459,208-17,462,465 , GRCh37.p13 chr9: 17,459,206-17,462,463 CNTLN
    nsv5866989copy number variation1nstd209human GRCh38 chr9: 17,244,874-17,248,273 , GRCh37.p13 chr9: 17,244,872-17,248,271 CNTLN
    nsv5866739copy number variation1nstd209human GRCh38 chr9: 17,190,557-17,207,132 , GRCh37.p13 chr9: 17,190,555-17,207,130 CNTLN
    nsv5866483copy number variation1nstd209human GRCh38 chr9: 17,175,855-17,180,123 , GRCh37.p13 chr9: 17,175,853-17,180,121 CNTLN
    nsv5866201copy number variation1nstd209human GRCh38 chr9: 17,228,239-17,238,373 , GRCh37.p13 chr9: 17,228,237-17,238,371 CNTLN
    nsv5866136copy number variation1nstd209human GRCh38 chr9: 17,433,351-17,445,288 , GRCh37.p13 chr9: 17,433,349-17,445,286 CNTLN, SAMM50P1
    nsv5866122copy number variation1nstd209human GRCh38 chr9: 17,409,716-17,416,515 , GRCh37.p13 chr9: 17,409,714-17,416,513 CNTLN
    nsv5866028copy number variation1nstd209human GRCh38 chr9: 17,359,580-17,365,466 , GRCh37.p13 chr9: 17,359,578-17,365,464 CNTLN
    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