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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944160copy number variation1nstd209human GRCh38 chr19: 39,288,671-39,297,593 , GRCh37.p13 chr19: 39,779,311-39,788,233 IFNL1
    nsv5871154copy number variation1nstd209human GRCh38 chr19: 39,288,705-39,297,567 , GRCh37.p13 chr19: 39,779,345-39,788,207 IFNL1
    nsv5027940copy number variation1nstd200human GRCh38 chr19: 39,292,030-39,294,966 , GRCh37.p13 chr19: 39,782,670-39,785,606 IFNL1
    nsv5027939copy number variation1nstd200human GRCh38 chr19: 39,288,615-39,297,518 , GRCh37.p13 chr19: 39,779,255-39,788,158 IFNL1
    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
    nsv4260823copy number variation1nstd166human GRCh37.p13 chr19: 39,782,681-39,785,643 , GRCh38.p12 chr19: 39,292,041-39,295,003 IFNL1
    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
    nsv3158769copy number variation1nstd151human GRCh37 chr19: 39,575,907-39,789,161 , GRCh38.p12 chr19: 39,085,267-39,298,521 IFNL1, SYCN, 9 more genes
    nsv3158716copy number variation1nstd151human GRCh37 chr19: 39,787,059-39,789,161 , GRCh38.p12 chr19: 39,296,419-39,298,521 IFNL1
    nsv2786827copy number variation1nstd132human NCBI36 chr19: 44,434,602-44,480,955 , GRCh37.p13 chr19: 39,742,762-39,789,115 , GRCh38.p12 chr19: 39,252,122-39,298,475 IFNL2, MSRB1P1, 2 more genes
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
    nsv2752158copy number variation1nstd130human GRCh37 chr19: 289,244-58,996,454 , GRCh38.p12 chr19: 289,244-58,485,087 , NFKBIB, 2456 more genes
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