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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv7057109inversion1nstd229human GRCh38 chr3: 46,623,487-46,754,784 , GRCh37.p13 chr3: 46,664,977-46,796,274 PRSS50, PRSS45P, 5 more genes
    nsv6716066copy number variation1nstd229human GRCh38 chr3: 46,686,696-46,686,793 , GRCh37.p13 chr3: 46,728,186-46,728,283 ALS2CL
    nsv6713511copy number variation1nstd229human GRCh38 chr3: 46,395,301-47,630,000 , GRCh37.p13 chr3: 46,436,792-47,671,490 BOLA2P2, LRRC2-AS1, 36 more genes
    nsv6708038copy number variation1nstd229human GRCh38 chr3: 46,664,401-46,667,600 , GRCh37.p13 chr3: 46,705,891-46,709,090 ALS2CL
    nsv6707678copy number variation1nstd229human GRCh38 chr3: 46,679,444-46,691,768 , GRCh37.p13 chr3: 46,720,934-46,733,258 ALS2CL
    nsv6707020copy number variation1nstd229human GRCh38 chr3: 46,664,258-46,667,837 , GRCh37.p13 chr3: 46,705,748-46,709,327 ALS2CL
    nsv6705131copy number variation1nstd229human GRCh38 chr3: 46,665,622-46,671,054 , GRCh37.p13 chr3: 46,707,112-46,712,544 ALS2CL
    nsv6701377copy number variation1nstd229human GRCh38 chr3: 46,663,401-46,667,800 , GRCh37.p13 chr3: 46,704,891-46,709,290 ALS2CL
    nsv6700069copy number variation1nstd229human GRCh38 chr3: 45,896,362-46,914,422 , GRCh37.p13 chr3: 45,937,854-46,955,912 LINC02009, ALS2CL, 32 more genes
    nsv6371926copy number variation1nstd223human GRCh38 chr3: 46,681,801-46,796,100 , GRCh37.p13 chr3: 46,723,291-46,837,590 PRSS45P, PRSS46P, 4 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6314975copy number variation1nstd102humanPathogenic GRCh37 chr3: 46,735,666-46,744,949 , GRCh38 chr3: 46,694,176-46,703,459 ALS2CL, TMIE
    nsv6290084copy number variation1nstd218human GRCh37 chr3: 46,667,314-46,754,514 , GRCh38.p12 chr3: 46,625,824-46,713,024 PRSS50, ALS2CL, 2 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5898801copy number variation1nstd209human GRCh38 chr3: 46,674,609-46,676,923 , GRCh37.p13 chr3: 46,716,099-46,718,413 ALS2CL
    nsv5895931copy number variation1nstd209human GRCh38 chr3: 46,664,251-46,667,834 , GRCh37.p13 chr3: 46,705,741-46,709,324 ALS2CL
    nsv5836563copy number variation1nstd209human GRCh38 chr3: 46,674,620-46,676,569 , GRCh37.p13 chr3: 46,716,110-46,718,059 ALS2CL
    nsv5835989copy number variation1nstd209human GRCh38 chr3: 46,664,208-46,667,812 , GRCh37.p13 chr3: 46,705,698-46,709,302 ALS2CL
    nsv5583417copy number variation1nstd207human GRCh38 chr3: 46,664,257-46,667,834 , GRCh37.p13 chr3: 46,705,747-46,709,324 ALS2CL
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