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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5586170copy number variation1nstd207human GRCh38 chr19: 39,196,680-39,196,753 , GRCh37.p13 chr19: 39,687,320-39,687,393 NCCRP1
    nsv5516465copy number variation1nstd206human GRCh38 chr19: 39,197,444-39,199,546 , GRCh37.p13 chr19: 39,688,084-39,690,186 NCCRP1
    nsv5375435translocation1nstd200human GRCh38 chr19: 39,197,694-39,197,694 , GRCh38 chr19: 39,199,545-39,199,545 , GRCh37.p13 chr19: 39,690,185-39,690,185 , GRCh37.p13 chr19: 39,688,334-39,688,334 NCCRP1
    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
    nsv4868330copy number variation1nstd200human GRCh37 chr19: 39,688,297-39,690,215 , GRCh38.p12 chr19: 39,197,657-39,199,575 NCCRP1
    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
    nsv4745961copy number variation1nstd199human GRCh37 chr19: 39,687,352-39,687,425 , GRCh38.p12 chr19: 39,196,712-39,196,785 NCCRP1
    nsv4671427copy number variation1nstd186human GRCh37 chr19: 39,688,261-39,690,208 , GRCh38.p12 chr19: 39,197,621-39,199,568 NCCRP1
    nsv4619272copy number variation1nstd183human GRCh37 chr19: 39,688,261-39,690,208 , GRCh38.p12 chr19: 39,197,621-39,199,568 NCCRP1
    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
    nsv4427142copy number variation1nstd174human GRCh37 chr19: 39,688,243-39,690,241 , GRCh38.p12 chr19: 39,197,603-39,199,601 NCCRP1
    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
    nsv3937449copy number variation1nstd167human GRCh37 chr19: 39,687,320-39,687,394 , GRCh38.p12 chr19: 39,196,680-39,196,754 NCCRP1
    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
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