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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 LRRC8E, ZNF414, 53 more genes
    nsv7066716inversion1nstd229human GRCh38 chr19: 6,518,017-8,344,162 , GRCh37.p13 chr19: 6,518,028-8,409,046 , STXBP2, 71 more genes
    nsv7062847inversion1nstd229human GRCh38 chr19: 7,473,530-8,349,302 , GRCh37.p13 chr19: 7,538,416-8,414,186 CERS4, LYPLA2P2, 47 more genes
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5297344copy number variation1nstd204human GRCh38.p13 chr19: 8,188,901-8,707,200 , GRCh37.p13 chr19: 8,253,785-8,634,914 RAB11B, HNRNPM, 17 more genes
    nsv5290897copy number variation1nstd204human GRCh38.p13 chr19: 8,275,201-8,449,800 , GRCh37.p13 chr19: 8,340,085-8,514,684 RAB11B-AS1, CD320, 9 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
    nsv4271799copy number variation1nstd166human GRCh37.p13 chr19: 8,384,000-8,389,000 , GRCh38.p12 chr19: 8,319,116-8,324,116 NDUFA7, KANK3, 1 more genes
    nsv4259084copy number variation1nstd166human GRCh37.p13 chr19: 8,277,752-8,457,787 , GRCh38.p12 chr19: 8,212,868-8,392,903 RAB11B, MIR4999, 9 more genes
    nsv3968074copy number variation1nstd168human GRCh38 chr19: 8,224,548-8,321,057 , GRCh37.p13 chr19: 8,289,432-8,385,941 NDUFA7, RPS28, 4 more genes
    nsv3921240copy number variation1nstd102humanUncertain significance NCBI36 chr19: 8,025,412-8,572,615 , GRCh37.p13 chr19: 8,119,412-8,666,615 , GRCh38.p12 chr19: 8,054,528-8,601,731 ADAMTS10, MIR4999, 18 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
    nsv3888397copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059 ELAVL1, MYO1F, 80 more genes
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