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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7077999inversion1nstd229human GRCh38 chr8: 90,977,597-95,722,625 , GRCh37.p13 chr8: 91,989,825-96,734,853 LINC02894, MIR3150B, 70 more genes
    nsv7077615inversion1nstd229human GRCh38 chr8: 94,663,509-94,663,611 , GRCh37.p13 chr8: 95,675,737-95,675,839 ESRP1
    nsv7072328inversion1nstd229human GRCh38 chr8: 94,696,256-94,702,688 , GRCh37.p13 chr8: 95,708,484-95,714,916 ESRP1
    nsv7072181inversion1nstd229human GRCh38 chr8: 94,465,642-98,351,757 , GRCh37.p13 chr8: 95,477,870-99,363,985 SDC2, LOC100286997, 59 more genes
    nsv7064838inversion1nstd229human GRCh38 chr8: 94,647,008-94,647,043 , GRCh37.p13 chr8: 95,659,236-95,659,271 ESRP1
    nsv6858051copy number variation1nstd229human GRCh38 chr8: 94,682,918-94,687,991 , GRCh37.p13 chr8: 95,695,146-95,700,219 ESRP1, RPS15AP26
    nsv6857424copy number variation1nstd229human GRCh38 chr8: 94,682,772-94,690,887 , GRCh37.p13 chr8: 95,695,000-95,703,115 ESRP1, RPS15AP26
    nsv6855818copy number variation1nstd229human GRCh38 chr8: 94,697,301-94,699,294 , GRCh37.p13 chr8: 95,709,529-95,711,522 ESRP1
    nsv6851933copy number variation1nstd229human GRCh38 chr8: 94,678,371-94,705,921 , GRCh37.p13 chr8: 95,690,599-95,718,149 ESRP1, RPS15AP26
    nsv6850532copy number variation1nstd229human GRCh38 chr8: 94,692,824-94,705,921 , GRCh37.p13 chr8: 95,705,052-95,718,149 ESRP1
    nsv6845444copy number variation1nstd229human GRCh38 chr8: 94,696,301-94,700,700 , GRCh37.p13 chr8: 95,708,529-95,712,928 ESRP1
    nsv6841253copy number variation1nstd229human GRCh38 chr8: 94,699,311-94,699,405 , GRCh37.p13 chr8: 95,711,539-95,711,633 ESRP1
    nsv6840920copy number variation1nstd229human GRCh38 chr8: 94,655,728-94,656,206 , GRCh37.p13 chr8: 95,667,956-95,668,434 ESRP1
    nsv6840584copy number variation1nstd229human GRCh38 chr8: 94,200,575-95,023,354 , GRCh37.p13 chr8: 95,212,803-96,035,582 NDUFAF6, FSBP, 18 more genes
    nsv6838589copy number variation1nstd229human GRCh38 chr8: 94,697,701-94,778,200 , GRCh37.p13 chr8: 95,709,929-95,790,428 DPY19L4, ESRP1
    nsv6838412copy number variation1nstd229human GRCh38 chr8: 94,696,961-94,705,923 , GRCh37.p13 chr8: 95,709,189-95,718,151 ESRP1
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6575396inversion1nstd223human GRCh38 chr8: 94,681,190-94,682,401 , GRCh37.p13 chr8: 95,693,418-95,694,629 ESRP1
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