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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5374708translocation1nstd200human GRCh38 chr16: 67,029,081-67,029,081 , GRCh38 chr19: 40,442,972-40,442,972 , GRCh37.p13 chr16: 67,062,984-67,062,984 , GRCh37.p13 chr19: 40,948,879-40,948,879 CBFB, SERTAD3, 1 more genes
    nsv5326580copy number variation1nstd204human GRCh38.p13 chr19: 40,438,645-40,439,819 , GRCh37.p13 chr19: 40,944,552-40,945,726 SERTAD3
    nsv5287129copy number variation1nstd204human GRCh38.p13 chr19: 40,119,401-40,793,500 , GRCh37.p13 chr19: 40,625,308-41,299,405 CCNP, SHKBP1, 28 more genes
    nsv5282080copy number variation1nstd204human GRCh38.p13 chr19: 40,437,810-40,440,659 , GRCh37.p13 chr19: 40,943,717-40,946,566 SERTAD3
    nsv5027996copy number variation1nstd200human GRCh38 chr19: 40,436,974-40,449,405 , GRCh37.p13 chr19: 40,942,881-40,955,312 BLVRB, SERTAD3-AS1, 1 more genes
    nsv5024637copy number variation1nstd200human GRCh38 chr19: 40,438,654-40,439,811 , GRCh37.p13 chr19: 40,944,561-40,945,718 SERTAD3
    nsv4868373copy number variation1nstd200human GRCh37 chr19: 40,942,881-40,955,312 , GRCh38.p12 chr19: 40,436,974-40,449,405 BLVRB, SERTAD3-AS1, 1 more genes
    nsv4865172copy number variation1nstd200human GRCh37 chr19: 40,944,561-40,945,718 , GRCh38.p12 chr19: 40,438,654-40,439,811 SERTAD3
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4262065copy number variation1nstd166human GRCh37.p13 chr19: 40,947,000-40,952,000 , GRCh38.p12 chr19: 40,441,093-40,446,093 BLVRB, SERTAD3, 1 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3895039copy number variation1nstd102humanBenign GRCh37 chr19: 40,636,400-41,060,616 , GRCh38.p12 chr19: 40,130,493-40,554,710 MIR6796, PLD3, 15 more genes
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3158935copy number variation1nstd151human GRCh37 chr19: 40,405,916-41,111,135 , GRCh38.p12 chr19: 39,906,247-40,605,229 , MIR6796, 26 more genes
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