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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5528649copy number variation1nstd206human GRCh38 chr19: 39,241,418-39,244,559 , GRCh37.p13 chr19: 39,732,058-39,735,199 IFNL3, IFNL4
    nsv5024626copy number variation1nstd200human GRCh38 chr19: 39,188,419-39,288,169 , GRCh37.p13 chr19: 39,679,059-39,778,809 IFNL3, SYCN, 6 more genes
    nsv4868332copy number variation1nstd200human GRCh37 chr19: 39,732,058-39,735,199 , GRCh38.p12 chr19: 39,241,418-39,244,559 IFNL4, IFNL3
    nsv4865165copy number variation1nstd200human GRCh37 chr19: 39,679,059-39,778,809 , GRCh38.p12 chr19: 39,188,419-39,288,169 IFNL2, NCCRP1, 6 more genes
    nsv4626207copy number variation1nstd183human GRCh37 chr19: 39,735,570-39,735,615 , GRCh38.p12 chr19: 39,244,930-39,244,975 IFNL3, IFNL4
    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
    nsv4270000copy number variation1nstd166human GRCh37.p13 chr19: 39,679,116-39,778,738 , GRCh38.p12 chr19: 39,188,476-39,288,098 IFNL2, IFNL3, 6 more genes
    nsv4253630copy number variation1nstd166human GRCh37.p13 chr19: 39,728,000-39,734,000 , GRCh38.p12 chr19: 39,237,360-39,243,360 IFNL3, IFNL3P1
    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
    nsv3912394copy number variation1nstd102humanUncertain significance NCBI36 chr19: 44,054,509-44,534,649 , GRCh37.p13 chr19: 39,362,669-39,842,809 , GRCh38.p12 chr19: 38,872,029-39,352,169 SAMD4B, IFNL1, 20 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
    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
    nsv3166915copy number variation1nstd151human GRCh37 chr19: 39,688,690-39,735,612 , GRCh38.p12 chr19: 39,198,050-39,244,972 SYCN, IFNL3P1, 3 more genes
    nsv3166824copy number variation1nstd151human GRCh37 chr19: 39,734,461-39,734,552 , GRCh38.p12 chr19: 39,243,821-39,243,912 IFNL3
    nsv3164310copy number variation1nstd151human GRCh37 chr19: 39,734,269-39,735,612 , GRCh38.p12 chr19: 39,243,629-39,244,972 IFNL3, IFNL4
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