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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6751365copy number variation1nstd229human GRCh38 chr4: 67,669,276-67,790,203 , GRCh37.p13 chr4: 68,534,994-68,655,921 GNRHR, LOC100419046, 6 more genes
    nsv6745238copy number variation1nstd229human GRCh38 chr4: 67,707,742-67,715,634 , GRCh37.p13 chr4: 68,573,460-68,581,352 ST3GAL1P1, UBA6-DT
    nsv6744253copy number variation1nstd229human GRCh38 chr4: 67,700,301-67,707,700 , GRCh37.p13 chr4: 68,566,019-68,573,418 UBA6, UBA6-DT
    nsv6743438copy number variation1nstd229human GRCh38 chr4: 67,701,688-67,707,665 , GRCh37.p13 chr4: 68,567,406-68,573,383 UBA6-DT
    nsv6739536copy number variation1nstd229human GRCh38 chr4: 67,706,865-67,707,213 , GRCh37.p13 chr4: 68,572,583-68,572,931 UBA6-DT
    nsv6637038copy number variation1nstd102humanUncertain significance GRCh37 chr4: 67,729,321-68,949,586 , GRCh38.p12 chr4: 66,863,603-68,083,868 UBA6-DT, LOC101927237, 24 more genes
    nsv6636883copy number variation1nstd102humanUncertain significance GRCh37 chr4: 66,215,872-68,647,080 , GRCh38.p12 chr4: 65,350,154-67,781,362 LOC100419046, LOC105377260, 24 more genes
    nsv6636728copy number variation1nstd102humanUncertain significance GRCh37 chr4: 68,485,743-69,138,293 , GRCh38.p12 chr4: 67,620,025-68,272,575 TMPRSS11D, LOC550113, 20 more genes
    nsv6629940copy number variation1nstd224human GRCh37 chr4: 68,453,189-68,704,036 , GRCh38.p12 chr4: 67,587,471-67,838,318 TMPRSS11CP, LOC107986207, 9 more genes
    nsv6395572copy number variation1nstd223human GRCh38 chr4: 67,700,701-67,701,400 , GRCh37.p13 chr4: 68,566,419-68,567,118 UBA6, UBA6-DT
    nsv6388106copy number variation1nstd223human GRCh38 chr4: 67,701,688-67,707,662 , GRCh37.p13 chr4: 68,567,406-68,573,380 UBA6-DT
    nsv6377046copy number variation1nstd223human GRCh38 chr4: 67,710,636-67,712,243 , GRCh37.p13 chr4: 68,576,354-68,577,961 UBA6-DT
    nsv6313845copy number variation1nstd102humanUncertain significance GRCh37 chr4: 68,272,006-68,923,410 , GRCh38.p12 chr4: 67,406,288-68,057,692 TMPRSS11F, TMPRSS11D, 20 more genes
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
    nsv6299384copy number variation1nstd186human GRCh37 chr4: 68,570,445-68,570,535 , GRCh38.p12 chr4: 67,704,727-67,704,817 UBA6-DT
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135600copy number variation1nstd213human GRCh37 chr4: 68,260,000-69,150,001 , GRCh38.p12 chr4: 67,394,282-68,284,283 TMPRSS11B, TMPRSS11BNL, 25 more genes
    nsv5898640copy number variation1nstd209human GRCh38 chr4: 67,701,686-67,707,661 , GRCh37.p13 chr4: 68,567,404-68,573,379 UBA6-DT
    nsv5840080copy number variation1nstd209human GRCh38 chr4: 67,701,683-67,707,834 , GRCh37.p13 chr4: 68,567,401-68,573,552 UBA6-DT
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
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