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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923212copy number variation1nstd209human GRCh38 chr8: 12,570,047-12,628,171 , GRCh37.p13 chr8: 12,427,556-12,485,680 LOC729732, RPS3AP34, 1 more genes
    nsv5922706copy number variation1nstd209human GRCh38 chr8: 12,566,737-12,624,769 , GRCh37.p13 chr8: 12,424,246-12,482,278 LOC729732, RPS3AP34, 1 more genes
    nsv5919739copy number variation1nstd209human GRCh38 chr8: 12,569,944-12,628,045 , GRCh37.p13 chr8: 12,427,453-12,485,554 LOC729732, RPS3AP34, 1 more genes
    nsv5908979copy number variation1nstd209human GRCh38 chr8: 12,570,301-12,575,325 , GRCh37.p13 chr8: 12,427,810-12,432,834 RPS3AP34, LOC729732
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5489375copy number variation1nstd206human GRCh38 chr8: 12,570,281-12,575,346 , GRCh37.p13 chr8: 12,427,790-12,432,855 RPS3AP34, LOC729732
    nsv5414186copy number variation1nstd206human GRCh38 chr8: 12,394,345-12,609,000 , GRCh37.p13 chr8: 12,251,854-12,466,509 FAM66A, ENPP7P6, 8 more genes
    nsv5387187copy number variation2nstd186human GRCh37 chr8: 12,427,810-12,432,835 , GRCh38.p12 chr8: 12,570,301-12,575,326 LOC729732, RPS3AP34
    nsv5312552copy number variation1nstd204human GRCh37.p13 chr8: 12,422,049-12,480,167 , GRCh38.p13 chr8: 12,564,540-12,622,658 LOC729732, RPS3AP34, 1 more genes
    nsv5305949copy number variation1nstd204human GRCh37.p13 chr8: 12,424,501-12,482,614 , GRCh38.p13 chr8: 12,566,992-12,625,105 LOC729732, RPS3AP34, 1 more genes
    nsv5305640copy number variation1nstd204human GRCh37.p13 chr8: 12,427,809-12,432,835 , GRCh38.p13 chr8: 12,570,300-12,575,326 LOC729732, RPS3AP34
    nsv5257975copy number variation1nstd204human GRCh38.p13 chr8: 12,496,301-12,604,300 , GRCh37.p13 chr8: 12,353,810-12,461,809 RPS3AP34, ENPP7P6, 2 more genes
    nsv5255110copy number variation1nstd204human GRCh38.p13 chr8: 12,570,255-12,575,241 , GRCh37.p13 chr8: 12,427,764-12,432,750 RPS3AP34, LOC729732
    nsv5254362copy number variation1nstd204human GRCh38.p13 chr8: 12,569,498-12,575,241 , GRCh37.p13 chr8: 12,427,007-12,432,750 RPS3AP34, LOC729732
    nsv5245633copy number variation1nstd204human GRCh38.p13 chr8: 12,521,501-12,570,300 , GRCh37.p13 chr8: 12,379,010-12,427,809 RPS3AP34, LOC729732, 1 more genes
    nsv5244090copy number variation1nstd204human GRCh38.p13 chr8: 12,538,201-12,570,300 , GRCh37.p13 chr8: 12,395,710-12,427,809 LOC729732, FAM86B2-DT, 1 more genes
    nsv5242040copy number variation1nstd204human GRCh38.p13 chr8: 12,521,301-12,598,600 , GRCh37.p13 chr8: 12,378,810-12,456,109 RPS3AP34, LOC729732, 1 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959132copy number variation1nstd200human GRCh38 chr8: 12,570,301-12,575,326 , GRCh37.p13 chr8: 12,427,810-12,432,835 LOC729732, RPS3AP34
    nsv4959131copy number variation1nstd200human GRCh38 chr8: 12,566,214-12,624,369 , GRCh37.p13 chr8: 12,423,723-12,481,878 RPS3AP34, FAM86B2-DT, 1 more genes
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