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Items: 1 to 20 of 145

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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
    nsv6737453copy number variation1nstd229human GRCh38 chr3: 186,585,388-186,585,528 , GRCh37.p13 chr3: 186,303,177-186,303,317 DNAJB11
    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
    nsv6360096copy number variation1nstd223human GRCh38 chr3: 186,584,509-186,585,167 , GRCh37.p13 chr3: 186,302,298-186,302,956 DNAJB11
    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
    nsv5198244mobile element insertion1nstd203human GRCh38 chr3: 186,576,633-186,576,633 , GRCh37.p13 chr3: 186,294,422-186,294,422 DNAJB11
    nsv5092679mobile element insertion1nstd203human GRCh38 chr3: 186,581,736-186,581,747 , GRCh37.p13 chr3: 186,299,525-186,299,536 DNAJB11
    nsv4798976copy number variation1nstd200human GRCh37 chr3: 186,291,487-186,291,973 , GRCh38.p12 chr3: 186,573,698-186,574,184 DNAJB11
    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
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