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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096902copy number variation3nstd102humanPathogenic GRCh37 chr2: 71,004,499-74,779,761 , GRCh38.p12 chr2: 70,777,367-74,552,634 TAF13P2, LOC107985897, 100 more genes
    nsv7096520copy number variation1nstd102humanUncertain significance GRCh37 chr2: 69,240,632-74,779,761 , GRCh38.p12 chr2: 69,013,500-74,552,634 LOC112268419, DQX1, 140 more genes
    nsv7058023inversion1nstd229human GRCh38 chr2: 70,984,842-71,331,695 , GRCh37.p13 chr2: 71,260,430-71,558,825 TRE-CTC15-1, MCEE, 11 more genes
    nsv6677122copy number variation1nstd229human GRCh38 chr2: 71,224,021-71,227,285 , GRCh37.p13 chr2: 71,451,151-71,454,415 PAIP2B
    nsv6674539copy number variation1nstd229human GRCh38 chr2: 71,184,701-71,195,500 , GRCh37.p13 chr2: 71,411,831-71,422,630 PAIP2B
    nsv6671140copy number variation1nstd229human GRCh38 chr2: 71,181,475-71,209,588 , GRCh37.p13 chr2: 71,408,605-71,436,718 PAIP2B
    nsv6662182copy number variation1nstd229human GRCh38 chr2: 71,184,401-71,246,800 , GRCh37.p13 chr2: 71,411,531-71,473,930 PAIP2B
    nsv6658154copy number variation1nstd229human GRCh38 chr2: 71,213,496-71,248,966 , GRCh37.p13 chr2: 71,440,626-71,476,096 PAIP2B
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628135copy number variation1nstd224human GRCh37 chr2: 71,311,643-71,409,350 , GRCh38.p12 chr2: 71,084,513-71,182,220 MPHOSPH10, MCEE, 1 more genes
    nsv6547422inversion1nstd223human GRCh38 chr2: 71,209,828-71,210,991 , GRCh37.p13 chr2: 71,436,958-71,438,121 PAIP2B
    nsv6543916inversion1nstd223human GRCh38 chr2: 71,200,472-71,201,408 , GRCh37.p13 chr2: 71,427,602-71,428,538 PAIP2B
    nsv6540618inversion1nstd223human GRCh38 chr2: 70,984,841-71,331,694 , GRCh37.p13 chr2: 71,260,430-71,558,824 ANKRD53, OR7E62P, 11 more genes
    nsv6354487copy number variation1nstd223human GRCh38 chr2: 71,208,852-71,209,331 , GRCh37.p13 chr2: 71,435,982-71,436,461 PAIP2B
    nsv6350041copy number variation1nstd223human GRCh38 chr2: 71,203,501-71,204,500 , GRCh37.p13 chr2: 71,430,631-71,431,630 PAIP2B
    nsv6345864copy number variation1nstd223human GRCh38 chr2: 71,186,865-71,187,376 , GRCh37.p13 chr2: 71,413,995-71,414,506 PAIP2B
    nsv6340492copy number variation1nstd223human GRCh38 chr2: 71,181,475-71,209,586 , GRCh37.p13 chr2: 71,408,605-71,436,716 PAIP2B
    nsv6340433copy number variation1nstd223human GRCh38 chr2: 71,191,908-71,200,711 , GRCh37.p13 chr2: 71,419,038-71,427,841 PAIP2B
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
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