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Items: 1 to 20 of 159

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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
    nsv6728648copy number variation1nstd229human GRCh38 chr3: 184,258,388-184,633,776 , GRCh37.p13 chr3: 183,976,176-184,351,564 LINC01840, CLCN2, 16 more genes
    nsv6726366copy number variation1nstd229human GRCh38 chr3: 184,370,553-184,444,193 , GRCh37.p13 chr3: 184,088,341-184,161,981 THPO, CHRD, 1 more genes
    nsv6723950copy number variation1nstd229human GRCh38 chr3: 184,388,006-184,406,721 , GRCh37.p13 chr3: 184,105,794-184,124,509 LINC02054, CHRD
    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
    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
    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
    nsv5905567copy number variation1nstd209human GRCh38 chr3: 184,388,237-184,388,392 , GRCh37.p13 chr3: 184,106,025-184,106,180 CHRD
    nsv5682875mobile element insertion1nstd211human GRCh38 chr3: 184,390,018-184,390,018 , GRCh37.p13 chr3: 184,107,806-184,107,806 CHRD
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5407517mobile element insertion1nstd206human GRCh38 chr3: 184,390,018-184,390,069 , GRCh37.p13 chr3: 184,107,806-184,107,857 CHRD
    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
    nsv4674171copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 183,789,584-186,034,649 , GRCh38.p12 chr3: 184,071,796-186,316,860 AP2M1, CLCN2, 54 more genes
    nsv4585428copy number variation1nstd183human GRCh37 chr3: 184,097,709-184,098,649 , GRCh38.p12 chr3: 184,379,921-184,380,861 THPO, CHRD
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