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Items: 1 to 20 of 211

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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
    nsv6717171copy number variation1nstd229human GRCh38 chr3: 46,442,520-46,444,404 , GRCh37.p13 chr3: 46,484,011-46,485,895 LTF
    nsv6714228copy number variation1nstd229human GRCh38 chr3: 46,465,709-46,466,096 , GRCh37.p13 chr3: 46,507,199-46,507,586 LTF
    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
    nsv6711644copy number variation1nstd229human GRCh38 chr3: 46,431,354-46,433,977 , GRCh37.p13 chr3: 46,472,845-46,475,468 LTF
    nsv6710425copy number variation1nstd229human GRCh38 chr3: 46,437,610-46,438,338 , GRCh37.p13 chr3: 46,479,101-46,479,829 LTF
    nsv6707829copy number variation1nstd229human GRCh38 chr3: 46,473,588-46,482,198 , GRCh37.p13 chr3: 46,515,078-46,523,688 LTF
    nsv6704926copy number variation1nstd229human GRCh38 chr3: 46,482,368-46,485,228 , GRCh37.p13 chr3: 46,523,858-46,526,718 LTF
    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
    nsv6374577copy number variation1nstd223human GRCh38 chr3: 46,442,520-46,444,404 , GRCh37.p13 chr3: 46,484,011-46,485,895 LTF
    nsv6373927copy number variation1nstd223human GRCh38 chr3: 46,462,313-46,462,333 , GRCh37.p13 chr3: 46,503,803-46,503,823 LTF
    nsv6369658copy number variation1nstd223human GRCh38 chr3: 46,433,915-46,659,106 , GRCh37.p13 chr3: 46,475,406-46,700,596 LRRC2-AS1, LTF, 4 more genes
    nsv6368803copy number variation1nstd223human GRCh38 chr3: 46,433,256-46,438,697 , GRCh37.p13 chr3: 46,474,747-46,480,188 LTF
    nsv6365953copy number variation1nstd223human GRCh38 chr3: 46,440,705-46,442,817 , GRCh37.p13 chr3: 46,482,196-46,484,308 LTF
    nsv6359681copy number variation1nstd223human GRCh38 chr3: 46,465,735-46,466,096 , GRCh37.p13 chr3: 46,507,225-46,507,586 LTF
    nsv6357471copy number variation1nstd223human GRCh38 chr3: 46,420,756-46,510,692 , GRCh37.p13 chr3: 46,462,247-46,552,182 LTF, LINC02009, 1 more genes
    nsv6355780copy number variation1nstd223human GRCh38 chr3: 46,448,843-46,452,734 , GRCh37.p13 chr3: 46,490,334-46,494,224 LTF
    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
    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
    nsv5993474copy number variation1nstd212human GRCh38 chr3: 46,441,902-46,441,965 , GRCh37.p13 chr3: 46,483,393-46,483,456 LTF
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