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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043354inversion1nstd229human GRCh38 chr3: 187,575,411-188,260,444 , GRCh37.p13 chr3: 187,293,199-187,978,232 LOC107986166, LPP, 10 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
    nsv6735061copy number variation1nstd229human GRCh38 chr3: 188,098,358-188,152,253 , GRCh37.p13 chr3: 187,816,146-187,870,041 LPP-AS2, LPP
    nsv6729714copy number variation1nstd229human GRCh38 chr3: 187,641,713-188,372,762 , GRCh37.p13 chr3: 187,359,501-188,090,550 BCL6, LOC105374265, 10 more genes
    nsv6724482copy number variation1nstd229human GRCh38 chr3: 188,146,421-188,284,686 , GRCh37.p13 chr3: 187,864,209-188,002,474 LPP-AS2, LPP, 1 more genes
    nsv6723451copy number variation1nstd229human GRCh38 chr3: 187,945,957-188,369,681 , GRCh37.p13 chr3: 187,663,745-188,087,469 LOC107986166, LPP, 3 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
    nsv6370544copy number variation1nstd223human GRCh38 chr3: 188,123,198-188,487,354 , GRCh37.p13 chr3: 187,840,986-188,205,142 LPP-AS2, LPP, 1 more genes
    nsv6362238copy number variation1nstd223human GRCh38 chr3: 188,146,421-188,284,686 , GRCh37.p13 chr3: 187,864,209-188,002,474 FLJ42393, LPP-AS2, 1 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
    nsv6134834copy number variation1nstd213human GRCh37 chr3: 187,860,000-187,990,001 , GRCh38.p12 chr3: 188,142,212-188,272,213 LPP, LPP-AS2, 1 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
    nsv4924981copy number variation1nstd200human GRCh38 chr3: 187,945,957-188,369,681 , GRCh37.p13 chr3: 187,663,745-188,087,469 LPP, LOC107986166, 3 more genes
    nsv4805075copy number variation1nstd200human GRCh37 chr3: 187,663,745-188,087,469 , GRCh38.p12 chr3: 187,945,957-188,369,681 LPP, LPP-AS2, 3 more genes
    nsv4679398copy number variation1nstd189human GRCh37.p13 chr3: 187,854,236-188,029,461 , GRCh38.p12 chr3: 188,136,448-188,311,673 LPP, LPP-AS2, 1 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
    nsv4673931copy number variation1nstd102humanUncertain significance GRCh37 chr3: 187,643,718-188,045,591 , GRCh38.p12 chr3: 187,925,930-188,327,803 LPP, LOC107986166, 4 more genes
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