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 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096951copy number variation2nstd102humanUncertain significance GRCh37 chr3: 186,256,485-187,009,420 , GRCh38.p12 chr3: 186,538,696-187,291,632 AHSG, ST6GAL1, 32 more genes
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6731232copy number variation1nstd229human GRCh38 chr3: 186,406,559-187,159,867 , GRCh37.p13 chr3: 186,124,348-186,877,655 PET100P1, SNORA81, 30 more genes
    nsv6636645copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 184,170,962-188,047,867 , GRCh38.p12 chr3: 184,453,174-188,330,079 AHSG, BCL6, 80 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6315366copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,556,940-188,083,060 , GRCh38.p12 chr3: 183,839,152-188,365,272 MASP1, PSMD10P2, 115 more genes
    nsv6313539copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147 ALG3, MIR4448, 133 more genes
    nsv6313504copy number variation1nstd102humanUncertain significance GRCh37 chr3: 186,149,060-186,599,706 , GRCh38.p12 chr3: 186,431,271-186,881,917 SNORD2, MIR1248, 25 more genes
    nsv6291381copy number variation1nstd102humanUncertain significance GRCh37 chr3: 186,056,143-186,306,541 , GRCh38.p12 chr3: 186,338,354-186,588,752 LINC02051, DNAJB11, 5 more genes
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv6134832copy number variation1nstd213human GRCh37 chr3: 185,970,000-186,760,001 , GRCh38.p12 chr3: 186,252,211-187,042,213 CRYGS, KNG1, 29 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv4728604copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971 LOC105374253, GPS2P2, 111 more genes
    nsv4728363copy number variation1nstd102humanUncertain significance GRCh37 chr3: 186,048,846-186,298,472 , GRCh38.p12 chr3: 186,331,057-186,580,683 LINC02051, CRYGS, 5 more genes
    nsv4683580copy number variation1nstd102humanPathogenic GRCh37 chr3: 186,256,465-187,009,440 , GRCh38.p12 chr3: 186,538,676-187,291,652 RPL39P19, FETUB, 32 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4674249copy number variation1nstd102humanPathogenic GRCh37 chr3: 185,879,162-187,446,035 , GRCh38.p12 chr3: 186,161,373-187,728,247 RTP1, RPL29P9, 43 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv3922577copy number variation1nstd102humanPathogenic GRCh37 chr3: 184,561,415-187,178,796 , GRCh38 chr3: 184,843,627-187,461,008 , NCBI36 chr3: 186,044,109-188,661,490 SNORA63, ADIPOQ-AS1, 59 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