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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973691inversion1nstd209human GRCh38 chr6: 6,312,424-9,433,879 , GRCh37.p13 chr6: 6,312,657-9,434,112 , BMP6, 45 more genes
    nsv5845700copy number variation1nstd209human GRCh38 chr6: 7,409,588-7,410,907 , GRCh37.p13 chr6: 7,409,821-7,411,140 RIOK1
    nsv5845438copy number variation1nstd209human GRCh38 chr6: 7,378,554-7,427,787 , GRCh37.p13 chr6: 7,378,787-7,428,020 RIOK1, CAGE1, 1 more genes
    nsv5089149mobile element insertion1nstd203human GRCh38 chr6: 7,398,763-7,398,774 , GRCh37.p13 chr6: 7,398,996-7,399,007 RIOK1
    nsv4947602copy number variation1nstd200human GRCh38 chr6: 7,388,217-7,390,201 , GRCh37.p13 chr6: 7,388,450-7,390,434 CAGE1, RIOK1
    nsv4934388copy number variation1nstd200human GRCh38 chr6: 7,374,110-7,399,755 , GRCh37.p13 chr6: 7,374,343-7,399,988 RIOK1, CAGE1
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4828478copy number variation1nstd200human GRCh37 chr6: 7,374,342-7,399,989 , GRCh38.p12 chr6: 7,374,109-7,399,756 RIOK1, CAGE1
    nsv4809586copy number variation1nstd200human GRCh37 chr6: 7,388,450-7,390,434 , GRCh38.p12 chr6: 7,388,217-7,390,201 RIOK1, CAGE1
    nsv4729577copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,495,789-8,070,987 , GRCh38.p12 chr6: 6,495,556-8,070,754 LOC105374904, RPS26P29, 30 more genes
    nsv4729451copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,874,846-7,396,438 , GRCh38.p12 chr6: 6,874,613-7,396,205 CAGE1, LOC105374904, 8 more genes
    nsv4675053copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,997,521-8,570,039 , GRCh38.p12 chr6: 5,997,288-8,569,806 BTF3P7, EEF1E1, 42 more genes
    nsv4674928copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,664,656-7,593,975 , GRCh38.p12 chr6: 6,664,423-7,593,742 LOC101928004, BTF3P7, 19 more genes
    nsv4593693copy number variation1nstd183human GRCh37 chr6: 7,354,509-7,442,731 , GRCh38.p12 chr6: 7,354,276-7,442,498 CAGE1, RIOK1, 1 more genes
    nsv4483957mobile element insertion1nstd166human GRCh37.p13 chr6: 7,392,665-7,392,665 , GRCh38.p12 chr6: 7,392,432-7,392,432 RIOK1
    nsv4457224copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,864,042-7,437,958 , GRCh38.p12 chr6: 6,863,809-7,437,725 LOC105374904, RREB1, 9 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456532copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,846,861-7,759,131 , GRCh38.p12 chr6: 6,846,628-7,758,898 RN7SL554P, RIOK1, 18 more genes
    nsv4410142copy number variation1nstd174human GRCh37 chr6: 7,408,653-7,452,835 , GRCh38.p12 chr6: 7,408,420-7,452,602 RIOK1, LOC102724234
    nsv4377278copy number variation1nstd173human GRCh37 chr6: 7,417,268-7,452,846 , GRCh38.p12 chr6: 7,417,035-7,452,613 RIOK1, LOC102724234
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