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    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
    nsv6720864copy number variation1nstd229human GRCh38 chr3: 186,786,474-186,794,820 , GRCh37.p13 chr3: 186,504,263-186,512,609 SNORA63, MIR1248, 5 more genes
    nsv6719141copy number variation1nstd229human GRCh38 chr3: 186,786,760-186,786,894 , GRCh37.p13 chr3: 186,504,549-186,504,683 SNORA63, MIR1248, 4 more genes
    nsv6718098copy number variation1nstd229human GRCh38 chr3: 186,784,216-186,959,926 , GRCh37.p13 chr3: 186,502,005-186,677,714 SNORA63B, LINC02043, 12 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
    nsv6628929copy number variation1nstd224human GRCh37 chr3: 186,328,121-186,710,637 , GRCh38.p12 chr3: 186,610,332-186,992,849 AHSG, EIF4A2, 21 more genes
    nsv6368922copy number variation1nstd223human GRCh38 chr3: 186,786,474-186,794,823 , GRCh37.p13 chr3: 186,504,263-186,512,612 SNORA4, SNORA81, 5 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
    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
    nsv6134797copy number variation1nstd213human GRCh37 chr3: 186,320,000-186,770,001 , GRCh38.p12 chr3: 186,602,211-187,052,213 KNG1, ADIPOQ, 21 more genes
    nsv5992284copy number variation1nstd212human GRCh38 chr3: 186,612,839-187,026,345 , GRCh37.p13 chr3: 186,330,628-186,744,133 , EIF4A2, 22 more genes
    nsv5992211copy number variation1nstd212human GRCh38 chr3: 186,784,217-186,959,925 , GRCh37.p13 chr3: 186,502,006-186,677,713 SNORA4, SNORA81, 12 more genes
    nsv5890328copy number variation1nstd209human GRCh37.p13 chr3: 186,504,549-186,504,682 , GRCh38 chr3: 186,786,760-186,786,893 EIF4A2, SNORA63, 4 more genes
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