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Items: 1 to 20 of 136

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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
    nsv7043383inversion1nstd229human GRCh38 chr3: 187,120,909-187,244,833 , GRCh37.p13 chr3: 186,838,697-186,962,621 RPL39L, RTP1, 4 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
    nsv6736766copy number variation1nstd229human GRCh38 chr3: 187,188,307-187,196,266 , GRCh37.p13 chr3: 186,906,095-186,914,054 RTP1, LOC101929106
    nsv6736371copy number variation1nstd229human GRCh38 chr3: 186,789,763-187,310,322 , GRCh37.p13 chr3: 186,507,552-187,028,110 RPS20P14, LOC101929106, 13 more genes
    nsv6734197copy number variation1nstd229human GRCh38 chr3: 187,190,201-187,283,400 , GRCh37.p13 chr3: 186,907,989-187,001,188 LOC105374260, RTP1, 2 more genes
    nsv6723744copy number variation1nstd229human GRCh38 chr3: 187,195,279-187,219,603 , GRCh37.p13 chr3: 186,913,067-186,937,391 MASP1, LOC101929106, 1 more genes
    nsv6718405copy number variation1nstd229human GRCh38 chr3: 187,200,355-187,200,383 , GRCh37.p13 chr3: 186,918,143-186,918,171 RTP1, LOC101929106
    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
    nsv6368310copy number variation1nstd223human GRCh38 chr3: 187,176,486-187,467,231 , GRCh37.p13 chr3: 186,894,274-187,185,019 LOC101929130, LINC02041, 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
    nsv6291270copy number variation1nstd102humanUncertain significance GRCh37 chr3: 186,830,759-187,192,352 , GRCh38.p12 chr3: 187,112,971-187,474,564 LINC02041, LOC101929106, 7 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
    nsv6134833copy number variation1nstd213human GRCh37 chr3: 186,910,000-193,810,001 , GRCh38.p12 chr3: 187,192,212-194,092,212 BCL6, LPP, 85 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
    nsv5318417copy number variation1nstd204human GRCh38.p13 chr3: 186,837,024-187,218,310 , GRCh37.p13 chr3: 186,554,813-186,936,098 RTP1, RPL39L, 8 more genes
    nsv4924979copy number variation1nstd200human GRCh38 chr3: 187,097,271-187,298,004 , GRCh37.p13 chr3: 186,815,059-187,015,792 RPL39L, RPL39P19, 5 more genes
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