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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096314copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,456,283-43,089,957 , GRCh38.p12 chr22: 42,060,279-42,693,951 SERHL2, POLDIP3, 28 more genes
    nsv7069304inversion1nstd229human GRCh38 chr22: 41,294,727-42,750,704 , GRCh37.p13 chr22: 41,690,731-43,146,710 SERHL2, CSDC2, 63 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7032574copy number variation1nstd229human GRCh38 chr22: 42,038,695-42,212,931 , GRCh37.p13 chr22: 42,434,699-42,608,937 TCF20, PHETA2, 13 more genes
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv6627476copy number variation2nstd224human GRCh37 chr22: 42,525,611-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 51,950-62,403 CYP2D7, CYP2D6, 1 more genes
    nsv6627475copy number variation2nstd224human GRCh37 chr22: 42,524,963-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 51,302-62,403 CYP2D6, LOC102723722, 1 more genes
    nsv6627474copy number variation1nstd224human GRCh37 chr22: 42,524,251-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 50,590-62,403 LOC102723722, CYP2D7, 1 more genes
    nsv6627473copy number variation1nstd224human GRCh37 chr22: 42,523,695-42,536,660 , GRCh38.p12 chr22|NT_187682.1: 50,034-62,999 CYP2D7, CYP2D6, 1 more genes
    nsv6627472copy number variation2nstd224human GRCh37 chr22: 42,523,695-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 50,034-62,403 CYP2D7, CYP2D6, 1 more genes
    nsv6627471copy number variation1nstd224human GRCh37 chr22: 42,523,678-42,536,294 , GRCh38.p12 chr22|NT_187682.1: 50,017-62,633 CYP2D7, CYP2D6, 1 more genes
    nsv6627470copy number variation16nstd224human GRCh37 chr22: 42,523,678-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 50,017-62,403 CYP2D6, CYP2D7, 1 more genes
    nsv6627469copy number variation1nstd224human GRCh37 chr22: 42,523,621-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 49,960-62,403 CYP2D7, CYP2D6, 1 more genes
    nsv6627468copy number variation7nstd224human GRCh37 chr22: 42,523,610-42,536,703 , GRCh38.p12 chr22|NT_187682.1: 49,949-63,042 CYP2D6, LOC102723722, 1 more genes
    nsv6627467copy number variation8nstd224human GRCh37 chr22: 42,523,314-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 49,653-62,403 CYP2D7, CYP2D6, 1 more genes
    nsv6627466copy number variation1nstd224human GRCh37 chr22: 42,523,247-42,536,703 , GRCh38.p12 chr22|NT_187682.1: 49,586-63,042 LOC102723722, CYP2D6, 1 more genes
    nsv6627465copy number variation7nstd224human GRCh37 chr22: 42,523,247-42,536,064 , GRCh38.p12 chr22|NT_187682.1: 49,586-62,403 CYP2D6, LOC102723722, 1 more genes
    nsv6627464copy number variation1nstd224human GRCh37 chr22: 42,523,184-42,537,623 , GRCh38.p12 chr22|NT_187682.1: 49,523-63,962 CYP2D6, LOC102723722, 1 more genes
    nsv6627463copy number variation1nstd224human GRCh37 chr22: 42,523,184-42,537,310 , GRCh38.p12 chr22|NT_187682.1: 49,523-63,649 CYP2D6, LOC102723722, 1 more genes
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