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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883040copy number variation1nstd102humanUncertain significance GRCh38 chr3: 179,198,750-179,234,712 , GRCh37 chr3: 178,916,538-178,952,500 PIK3CA
    nsv5381361copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,916,608-178,952,158 , GRCh38.p12 chr3: 179,198,820-179,234,370 PIK3CA
    nsv6311863copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,916,614-178,952,152 , GRCh38.p12 chr3: 179,198,826-179,234,364 PIK3CA
    nsv4682918copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,917,468-178,952,162 , GRCh38.p12 chr3: 179,199,680-179,234,374 PIK3CA
    nsv4683932copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,921,322-178,952,152 , GRCh38.p12 chr3: 179,203,534-179,234,364 PIK3CA
    nsv5381415copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,935,988-178,952,152 , GRCh38.p12 chr3: 179,218,200-179,234,364 PIK3CA
    nsv4454576copy number variation1nstd102humanUncertain significance GRCh38 chr3: 179,224,071-179,234,374 , GRCh37 chr3: 178,941,859-178,952,162 PIK3CA
    nsv6311864copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,951,872-178,952,152 , GRCh38.p12 chr3: 179,234,084-179,234,364 PIK3CA
    nsv6636803copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,755,126-178,842,215 , GRCh38.p12 chr3: 179,037,338-179,124,427 ZMAT3, PIK3CA-DT
    nsv3882658copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,917,597-179,094,773 , GRCh38.p12 chr3: 179,199,809-179,376,985 PIK3CA, KCNMB3, 3 more genes
    nsv3913254copy number variation1nstd102humanPathogenic NCBI36 chr3: 175,313,014-183,652,825 , GRCh37.p13 chr3: 173,830,320-182,170,131 , GRCh38.p12 chr3: 174,112,530-182,452,343 PIK3CA, RNU6-486P, 88 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 PIK3CA, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 PIK3CA, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 PIK3CA, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 PIK3CA, LINC02614, 1469 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 PIK3CA, LOC105374179, 785 more genes
    nsv3874894copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426 PIK3CA, RNU6-901P, 673 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 PIK3CA, LOC105374260, 696 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 PIK3CA, LINC02031, 647 more genes
    nsv3913128copy number variation1nstd102humanPathogenic GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323 PIK3CA, SNORA4, 644 more genes
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