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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6935163copy number variation1nstd229human GRCh38 chr12: 120,067,201-120,694,800 , GRCh37.p13 chr12: 120,505,005-121,132,603 RPL11P5, RNF10, 30 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6930227copy number variation1nstd229human GRCh38 chr12: 120,250,901-120,560,500 , GRCh37.p13 chr12: 120,688,704-120,998,303 RNU6-1088P, RNF10, 17 more genes
    nsv6930083copy number variation1nstd229human GRCh38 chr12: 120,251,001-120,606,400 , GRCh37.p13 chr12: 120,688,804-121,044,203 COX6A1, NRAV, 19 more genes
    nsv6927714copy number variation1nstd229human GRCh38 chr12: 120,274,920-120,281,541 , GRCh37.p13 chr12: 120,712,723-120,719,344 NME2P1
    nsv6919599copy number variation1nstd229human GRCh38 chr12: 119,989,801-120,740,500 , GRCh37.p13 chr12: 120,427,605-121,178,303 RPS20P31, MLEC, 33 more genes
    nsv6919305copy number variation1nstd229human GRCh38 chr12: 120,278,345-120,283,365 , GRCh37.p13 chr12: 120,716,148-120,721,168 NME2P1
    nsv6637895copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,665,945-120,951,612 , GRCh38.p12 chr12: 120,228,142-120,513,809 SIRT4, RPS20P31, 16 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6582212inversion1nstd223human GRCh38 chr12: 120,279,817-120,280,598 , GRCh37.p13 chr12: 120,717,620-120,718,401 NME2P1
    nsv6486607copy number variation1nstd223human GRCh38 chr12: 120,273,243-120,285,500 , GRCh37.p13 chr12: 120,711,046-120,723,303 NME2P1
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6132411copy number variation1nstd213human GRCh37 chr12: 119,880,000-120,880,001 , GRCh38.p12 chr12: 119,442,195-120,442,198 MSI1, RPLP0, 25 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5502735copy number variation1nstd206human GRCh38 chr12: 120,281,648-120,285,649 , GRCh37.p13 chr12: 120,719,451-120,723,452 NME2P1
    nsv4995965copy number variation1nstd200human GRCh38 chr12: 120,282,552-120,290,360 , GRCh37.p13 chr12: 120,720,355-120,728,163 NME2P1, RNU4-2, 1 more genes
    nsv4995964copy number variation1nstd200human GRCh38 chr12: 120,280,533-120,285,993 , GRCh37.p13 chr12: 120,718,336-120,723,796 NME2P1
    nsv4995963copy number variation1nstd200human GRCh38 chr12: 120,278,345-120,283,359 , GRCh37.p13 chr12: 120,716,148-120,721,162 NME2P1
    nsv4995962copy number variation1nstd200human GRCh38 chr12: 120,273,257-120,285,524 , GRCh37.p13 chr12: 120,711,060-120,723,327 NME2P1
    nsv4843322copy number variation1nstd200human GRCh37 chr12: 120,720,352-120,728,164 , GRCh38.p12 chr12: 120,282,549-120,290,361 RNU4-2, SIRT4, 1 more genes
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