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Items: 1 to 20 of 680

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7076476inversion1nstd229human GRCh38 chr12: 27,630,230-27,633,327 , GRCh37.p13 chr12: 27,783,163-27,786,260 PPFIBP1
    nsv7075067inversion1nstd229human GRCh38 chr12: 27,595,117-27,595,238 , GRCh37.p13 chr12: 27,748,050-27,748,171 PPFIBP1
    nsv7063256inversion1nstd229human GRCh38 chr12: 25,590,859-27,919,674 , GRCh37.p13 chr12: 25,743,793-28,072,607 RARS1P1, LOC101929091, 34 more genes
    nsv6937693copy number variation1nstd229human GRCh38 chr12: 27,131,001-27,643,400 , GRCh37.p13 chr12: 27,283,934-27,796,333 BMAL2, STK38L, 5 more genes
    nsv6935087copy number variation1nstd229human GRCh38 chr12: 26,967,401-27,843,600 , GRCh37.p13 chr12: 27,120,334-27,996,533 RARS1P1, RN7SKP15, 16 more genes
    nsv6932567copy number variation1nstd229human GRCh38 chr12: 27,563,585-27,572,435 , GRCh37.p13 chr12: 27,716,518-27,725,368 PPFIBP1
    nsv6932106copy number variation1nstd229human GRCh38 chr12: 27,131,201-27,643,400 , GRCh37.p13 chr12: 27,284,134-27,796,333 BMAL2, C12orf71BP, 5 more genes
    nsv6930887copy number variation1nstd229human GRCh38 chr12: 27,603,209-27,606,758 , GRCh37.p13 chr12: 27,756,142-27,759,691 PPFIBP1
    nsv6930180copy number variation1nstd229human GRCh38 chr12: 27,619,923-27,619,991 , GRCh37.p13 chr12: 27,772,856-27,772,924 PPFIBP1
    nsv6929100copy number variation1nstd229human GRCh38 chr12: 27,620,695-27,620,723 , GRCh37.p13 chr12: 27,773,628-27,773,656 PPFIBP1
    nsv6928344copy number variation1nstd229human GRCh38 chr12: 27,477,188-27,641,266 , GRCh37.p13 chr12: 27,630,121-27,794,199 C12orf71BP, RARS1P1, 2 more genes
    nsv6926735copy number variation1nstd229human GRCh38 chr12: 27,604,501-27,613,000 , GRCh37.p13 chr12: 27,757,434-27,765,933 PPFIBP1
    nsv6926343copy number variation1nstd229human GRCh38 chr12: 27,243,201-28,097,100 , GRCh37.p13 chr12: 27,396,134-28,250,033 RARS1P1, PPFIBP1, 15 more genes
    nsv6924665copy number variation1nstd229human GRCh38 chr12: 27,558,080-27,568,569 , GRCh37.p13 chr12: 27,711,013-27,721,502 PPFIBP1
    nsv6918917copy number variation1nstd229human GRCh38 chr12: 27,549,197-27,549,243 , GRCh37.p13 chr12: 27,702,130-27,702,176 PPFIBP1
    nsv6918674copy number variation1nstd229human GRCh38 chr12: 27,609,638-27,609,989 , GRCh37.p13 chr12: 27,762,571-27,762,922 PPFIBP1
    nsv6621451copy number variation1nstd224human GRCh37 chr12: 27,783,723-27,820,498 , GRCh38.p12 chr12: 27,630,790-27,667,565 PPFIBP1
    nsv6621450copy number variation1nstd224human GRCh37 chr12: 27,304,878-27,799,019 , GRCh38.p12 chr12: 27,151,945-27,646,086 PPFIBP1, STK38L, 5 more genes
    nsv6594034inversion1nstd223human GRCh38 chr12: 27,630,230-27,633,327 , GRCh37.p13 chr12: 27,783,163-27,786,260 PPFIBP1
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