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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6735393copy number variation1nstd229human GRCh38 chr3: 184,563,652-184,715,549 , GRCh37.p13 chr3: 184,281,440-184,433,337 LOC107986163, EPHB3, 1 more genes
    nsv6727573copy number variation1nstd229human GRCh38 chr3: 184,673,501-184,737,700 , GRCh37.p13 chr3: 184,391,289-184,455,488 MAGEF1, LOC107986163
    nsv6722552copy number variation1nstd229human GRCh38 chr3: 184,709,004-184,719,615 , GRCh37.p13 chr3: 184,426,792-184,437,403 MAGEF1, LOC107986163
    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
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 PRICKLE1P1, KLHL24, 99 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
    nsv6372393copy number variation1nstd223human GRCh38 chr3: 184,709,003-184,719,614 , GRCh37.p13 chr3: 184,426,791-184,437,402 MAGEF1, LOC107986163
    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
    nsv6295982copy number variation1nstd186human GRCh37 chr3: 184,415,651-184,427,925 , GRCh38.p12 chr3: 184,697,863-184,710,137 MAGEF1
    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
    nsv6134831copy number variation1nstd213human GRCh37 chr3: 184,100,000-184,800,001 , GRCh38.p12 chr3: 184,382,212-185,082,213 CHRD, MAGEF1, 10 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
    nsv5442633copy number variation1nstd206human GRCh38 chr3: 184,697,863-184,710,137 , GRCh37.p13 chr3: 184,415,651-184,427,925 MAGEF1
    nsv4798927copy number variation1nstd200human GRCh37 chr3: 184,415,651-184,427,925 , GRCh38.p12 chr3: 184,697,863-184,710,137 MAGEF1
    nsv4769252copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303 LOC107986054, LOC107986160, 83 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
    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
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