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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932060copy number variation1nstd209human GRCh38 chr19: 7,886,306-7,887,141 , GRCh37.p13 chr19: 7,951,191-7,952,026 RNA5SP463, LRRC8E
    nsv5531214copy number variation1nstd206human GRCh38 chr19: 7,886,277-7,887,181 , GRCh37.p13 chr19: 7,951,162-7,952,066 LRRC8E, RNA5SP463
    nsv5522383copy number variation1nstd206human GRCh38 chr19: 7,894,349-7,894,692 , GRCh37.p13 chr19: 7,959,234-7,959,577 LRRC8E
    nsv5522062copy number variation1nstd206human GRCh38 chr19: 7,891,636-7,892,882 , GRCh37.p13 chr19: 7,956,521-7,957,767 LRRC8E
    nsv5027589copy number variation1nstd200human GRCh38 chr19: 7,897,311-7,898,471 , GRCh37.p13 chr19: 7,962,196-7,963,356 LRRC8E
    nsv5027588copy number variation1nstd200human GRCh38 chr19: 7,889,424-7,890,718 , GRCh37.p13 chr19: 7,954,309-7,955,603 LRRC8E
    nsv5027587copy number variation1nstd200human GRCh38 chr19: 7,886,325-7,887,133 , GRCh37.p13 chr19: 7,951,210-7,952,018 LRRC8E, RNA5SP463
    nsv4748720copy number variation1nstd199human GRCh37 chr19: 7,951,192-7,952,027 , GRCh38.p12 chr19: 7,886,307-7,887,142 RNA5SP463, LRRC8E
    nsv4682037copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310 XAB2, CLEC4G, 40 more genes
    nsv4676269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878 LRRC8E, CLEC4GP1, 47 more genes
    nsv4260440copy number variation1nstd166human GRCh37.p13 chr19: 7,953,043-7,955,833 , GRCh38.p12 chr19: 7,888,158-7,890,948 LRRC8E
    nsv4257823copy number variation1nstd166human GRCh37.p13 chr19: 7,957,345-7,961,119 , GRCh38.p12 chr19: 7,892,460-7,896,234 LRRC8E
    nsv3956041copy number variation1nstd168human GRCh38 chr19: 7,859,413-7,901,845 , GRCh37.p13 chr19: 7,924,299-7,966,730 MAP2K7, LRRC8E, 4 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 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
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 PCP2, EIF1P6, 250 more genes
    nsv3165763copy number variation1nstd151human GRCh37 chr19: 7,504,825-8,155,140 , GRCh38.p12 chr19: 7,439,939-8,090,256 SAXO5, LYPLA2P2, 39 more genes
    nsv3165096copy number variation1nstd151human GRCh37 chr19: 7,960,486-8,531,277 , GRCh38.p12 chr19: 7,895,601-8,466,393 RAB11B, FBN3, 22 more genes
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