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 225

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5632443insertion1nstd207human GRCh38 chr6: 170,160,516-170,160,516 , GRCh37.p13 chr6: 170,475,740-170,475,740 LOC102724511, LOC105378153
    nsv5568485copy number variation1nstd207human GRCh38 chr6: 170,160,490-170,160,587 , GRCh37.p13 chr6: 170,475,714-170,475,811 LOC102724511, LOC105378153
    nsv5461415copy number variation1nstd206human GRCh38 chr6: 170,160,635-170,160,744 , GRCh37.p13 chr6: 170,475,859-170,475,968 LOC105378153, LOC102724511
    nsv5305606copy number variation1nstd204human GRCh38.p13 chr6: 170,056,994-170,362,978 , GRCh37.p13 chr6: 170,372,218-170,672,066 MIR4644, LINC01624, 8 more genes
    nsv5228321copy number variation1nstd204human GRCh38.p13 chr6: 170,141,308-170,161,802 , GRCh37.p13 chr6: 170,456,532-170,477,026 LOC101929614, LOC102724511, 1 more genes
    nsv4824924copy number variation1nstd200human GRCh37 chr6: 170,372,228-170,672,064 , GRCh38.p12 chr6: 170,057,004-170,362,976 RPL12P23, LOC285804, 8 more genes
    nsv4747811copy number variation1nstd199human GRCh37 chr6: 170,475,714-170,475,780 , GRCh38.p12 chr6: 170,160,490-170,160,556 LOC105378153, LOC102724511
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4729261copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,580,012-170,919,482 , GRCh38.p12 chr6: 167,166,524-170,610,394 LOC107986549, AFDN, 81 more genes
    nsv4675958copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,440,417-170,919,482 , GRCh38.p12 chr6: 167,026,929-170,610,394 CCR6, HGC6.3, 86 more genes
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
    nsv4675577copy number variation1nstd102humanPathogenic GRCh37 chr6: 170,136,337-170,919,482 , GRCh38.p12 chr6: 169,736,241-170,610,394 LOC107986676, LOC105378149, 22 more genes
    nsv4675360copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 170,331,096-170,919,482 , GRCh38.p12 chr6: 170,015,872-170,610,394 PDCD2, PSMB1, 14 more genes
    nsv4675300copy number variation1nstd102humanUncertain significance GRCh37 chr6: 170,356,782-170,618,134 , GRCh38.p12 chr6: 170,041,558-170,309,046 LOC105378153, RPL12P23, 7 more genes
    nsv4675281copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394 LOC105378127, LOC105378130, 148 more genes
    nsv4455397copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,607,593-170,919,482 , GRCh38.p12 chr6: 166,194,105-170,610,394 TBP, LOC112267970, 108 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4376081copy number variation1nstd173human GRCh37 chr6: 163,617,482-170,919,482 , GRCh38.p12 chr6: 163,196,450-170,610,394 , LOC107986550, 151 more genes
    nsv4350147copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,311,806-170,881,789 , GRCh38.p12 chr6: 167,911,126-170,572,701 LINC00574, LOC107986674, 56 more genes
    nsv4349604copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,517,762-170,919,470 , GRCh38.p12 chr6: 166,104,274-170,610,382 LOC105378145, FRMD1, 109 more genes
    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