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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145409insertion1nstd232human GRCh37.p13 chr1: 17,355,232-17,355,232 , GRCh38.p12 chr1: 17,028,737-17,028,737 SDHB
    nsv7138651insertion1nstd232human GRCh37.p13 chr1: 17,350,573-17,350,573 , GRCh38.p12 chr1: 17,024,078-17,024,078 SDHB
    nsv7099180copy number variation1nstd231human GRCh38.p12 chr1: 17,015,046-18,804,744 , GRCh37 chr1: 17,341,541-19,131,238 PAX7, SDHB, 19 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095765copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 17,359,545-17,359,650 , GRCh38.p12 chr1: 17,033,050-17,033,155 SDHB
    nsv7095713copy number variation1nstd102humanPathogenic GRCh37 chr1: 17,359,545-17,380,514 , GRCh38.p12 chr1: 17,033,050-17,054,019 SDHB
    nsv7095563copy number variation1nstd102humanUncertain significance GRCh37 chr1: 17,354,234-17,354,370 , GRCh38.p12 chr1: 17,027,739-17,027,875 SDHB
    nsv7095489copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 17,371,256-17,371,383 , GRCh38.p12 chr1: 17,044,761-17,044,888 SDHB
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv7042425inversion1nstd229human GRCh38 chr1: 17,036,929-17,039,332 , GRCh37.p13 chr1: 17,363,424-17,365,827 SDHB
    nsv6644556copy number variation1nstd229human GRCh38 chr1: 17,048,753-17,064,428 , GRCh37.p13 chr1: 17,375,248-17,390,923 SDHB
    nsv6644537copy number variation1nstd229human GRCh38 chr1: 16,997,179-17,021,733 , GRCh37.p13 chr1: 17,323,674-17,348,228 ATP13A2, SDHB
    nsv6644053copy number variation1nstd229human GRCh38 chr1: 17,034,509-17,036,846 , GRCh37.p13 chr1: 17,361,004-17,363,341 SDHB
    nsv6637160copy number variation1nstd102humanUncertain significance GRCh37 chr1: 17,366,386-17,491,556 , GRCh38.p12 chr1: 17,039,891-17,165,061 PADI2, SDHB, 1 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6625881copy number variation1nstd224human GRCh37 chr1: 17,371,253-17,436,661 , GRCh38.p12 chr1: 17,044,758-17,110,166 PADI2, SDHB
    nsv6625681copy number variation1nstd224human GRCh37 chr1: 17,316,686-17,380,483 , GRCh38.p12 chr1: 16,990,191-17,053,988 ATP13A2, SDHB
    nsv6552449inversion1nstd223human GRCh38 chr1: 17,041,526-17,043,095 , GRCh37.p13 chr1: 17,368,021-17,369,590 SDHB
    nsv6540602inversion1nstd223human GRCh38 chr1: 17,046,749-17,047,197 , GRCh37.p13 chr1: 17,373,244-17,373,692 SDHB
    nsv6325982copy number variation1nstd223human GRCh38 chr1: 16,989,078-17,061,247 , GRCh37.p13 chr1: 17,315,573-17,387,742 ATP13A2, SDHB
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