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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 PLCL2, LOC102724104, 291 more genes
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 PLCL2, RNU6-905P, 99 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 PLCL2, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 PLCL2, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 PLCL2, RPL23AP49, 2875 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 PLCL2, LINC02022, 540 more genes
    nsv3876280copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973 PLCL2, OXTR, 460 more genes
    nsv3892895copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571 PLCL2, RPL34P11, 452 more genes
    nsv3878718copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690 PLCL2, LRRC3B, 436 more genes
    nsv3875913copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709 PLCL2, RPS27P11, 424 more genes
    nsv3901059copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703 PLCL2, RPL32, 369 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 PLCL2, RNU6-243P, 382 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 PLCL2, RN7SL4P, 348 more genes
    nsv3875223copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-24,432,821 , GRCh38.p12 chr3: 20,213-24,391,330 PLCL2, XPC-AS1, 311 more genes
    nsv3904668copy number variation1nstd102humanPathogenic NCBI36 chr3: 48,914-20,350,883 , GRCh37 chr3: 73,914-20,375,879 , GRCh38 chr3: 32,241-20,334,387 PLCL2, C3orf20, 281 more genes
    nsv3907461copy number variation1nstd102humanPathogenic GRCh38 chr3: 63,843-19,510,600 , GRCh37 chr3: 105,526-19,552,092 , NCBI36 chr3: 80,526-19,527,096 PLCL2, TAMM41, 267 more genes
    nsv3885029copy number variation1nstd102humanPathogenic GRCh37 chr3: 1,897,972-19,519,085 , GRCh38.p12 chr3: 1,856,288-19,477,593 PLCL2, VGLL4, 247 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 PLCL2, TMEM43, 132 more genes
    nsv3888298copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,276,005-24,295,240 , GRCh38.p12 chr3: 13,234,505-24,253,749 PLCL2, NR1D2, 134 more genes
    nsv3919322copy number variation1nstd102humanPathogenic GRCh38 chr3: 14,360,747-21,656,134 , GRCh37 chr3: 14,402,247-21,697,626 , NCBI36 chr3: 14,377,251-21,672,630 PLCL2, LOC105376988, 89 more genes
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