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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5695770mobile element insertion2nstd211human GRCh38 chr8: 56,645,082-56,645,082 , GRCh37.p13 chr8: 57,557,641-57,557,641 LOC105375851
    nsv5413686mobile element insertion1nstd206human GRCh38 chr8: 56,645,082-56,645,133 , GRCh37.p13 chr8: 57,557,641-57,557,692 LOC105375851
    nsv5371699translocation1nstd200human GRCh38 chr8: 56,657,370-56,657,370 , GRCh38 chr8: 56,656,755-56,656,755 , GRCh37.p13 chr8: 57,569,314-57,569,314 , GRCh37.p13 chr8: 57,569,929-57,569,929 LOC105375851
    nsv5371698translocation1nstd200human GRCh38 chr8: 56,640,743-56,640,743 , GRCh38 chr8: 56,639,209-56,639,209 , GRCh37.p13 chr8: 57,551,768-57,551,768 , GRCh37.p13 chr8: 57,553,302-57,553,302 LOC105375851
    nsv5371697translocation1nstd200human GRCh38 chr8: 56,638,825-56,638,825 , GRCh38 chr8: 56,640,727-56,640,727 , GRCh37.p13 chr8: 57,553,286-57,553,286 , GRCh37.p13 chr8: 57,551,384-57,551,384 LOC105375851
    nsv5341934translocation1nstd200human GRCh37 chr8: 57,569,929-57,569,929 , GRCh37 chr8: 57,569,314-57,569,314 , GRCh38.p12 chr8: 56,656,755-56,656,755 , GRCh38.p12 chr8: 56,657,370-56,657,370 LOC105375851
    nsv5117517mobile element insertion1nstd203human GRCh38 chr8: 56,645,067-56,645,082 , GRCh37.p13 chr8: 57,557,626-57,557,641 LOC105375851
    nsv4952461copy number variation1nstd200human GRCh38 chr8: 56,655,703-56,655,821 , GRCh37.p13 chr8: 57,568,262-57,568,380 LOC105375851
    nsv4952460copy number variation1nstd200human GRCh38 chr8: 56,649,505-56,649,678 , GRCh37.p13 chr8: 57,562,064-57,562,237 LOC105375851
    nsv4813199copy number variation1nstd200human GRCh37 chr8: 57,568,262-57,568,380 , GRCh38.p12 chr8: 56,655,703-56,655,821 LOC105375851
    nsv4496216mobile element insertion1nstd166human GRCh37.p13 chr8: 57,557,626-57,557,626 , GRCh38.p12 chr8: 56,645,067-56,645,067 LOC105375851
    nsv4488132mobile element insertion1nstd166human GRCh37.p13 chr8: 57,550,620-57,550,620 , GRCh38.p12 chr8: 56,638,061-56,638,061 LOC105375851
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4166236copy number variation1nstd166human GRCh37.p13 chr8: 57,556,195-57,556,320 , GRCh38.p12 chr8: 56,643,636-56,643,761 LOC105375851
    nsv4155692copy number variation1nstd166human GRCh37.p13 chr8: 57,569,076-57,569,929 , GRCh38.p12 chr8: 56,656,517-56,657,370 LOC105375851
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 LOC105375849, RP1, 103 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
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