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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7092109copy number variation1nstd229human GRCh38 chrX: 57,906,033-57,910,842 , GRCh37.p13 chrX: 57,932,467-57,937,276 ZXDA
    nsv7092108copy number variation1nstd229human GRCh38 chrX: 57,896,401-57,906,100 , GRCh37.p13 chrX: 57,922,835-57,932,534 ZXDA
    nsv7092073copy number variation1nstd229human GRCh38 chrX: 57,676,197-57,994,729 , GRCh37.p13 chrX: 57,702,630-58,021,163 MYCLP2, KRT8P17, 3 more genes
    nsv7088231copy number variation1nstd229human GRCh38 chrX: 57,216,637-57,999,292 , GRCh37.p13 chrX: 57,243,070-58,025,726 KRT8P17, ZXDA, 8 more genes
    nsv7081251copy number variation1nstd229human GRCh38 chrX: 56,856,775-57,906,091 , GRCh37.p13 chrX: 56,883,208-57,932,525 MDH1P1, ZXDA, 10 more genes
    nsv7024182inversion1nstd229human GRCh38 chrX: 55,283,275-57,909,590 , GRCh37.p13 chrX: 55,309,708-57,936,024 UBQLN2, USP51, 27 more genes
    nsv6636248copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 53,731,940-63,932,866 , GRCh38.p12 chrX: 53,704,997-64,712,986 ALAS2, FGD1, 89 more genes
    nsv6636004copy number variation1nstd102humanPathogenic GRCh38 chrX: 57,537,466-65,512,709 , GRCh37.p13 chrX: 57,563,899-64,732,589 ZC4H2, ZC3H12B, 43 more genes
    nsv6634261copy number variation1nstd224human GRCh37 chrX: 56,889,389-58,389,872 , GRCh38.p12 chrX: 56,862,956-58,363,439 SPIN3, NLRP2B, 12 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634159copy number variation1nstd224human GRCh37 chrX: 57,928,734-58,403,144 , GRCh38.p12 chrX: 57,902,300-58,376,711 KRT8P17, ZXDA, 1 more genes
    nsv6634158copy number variation1nstd224human GRCh37 chrX: 57,628,448-58,403,144 , GRCh38.p12 chrX: 57,602,015-58,376,711 ZXDA, NLRP2B, 4 more genes
    nsv6633884copy number variation1nstd224human GRCh37 chrX: 57,802,424-58,403,144 , GRCh38.p12 chrX: 57,775,991-58,376,711 ZXDA, MYCLP2, 1 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6137619copy number variation1nstd213human GRCh37 chrX: 52,520,000-58,560,001 , GRCh38.p12 chrX: 52,523,686-58,533,568 ACTG1P10, ALAS2, 106 more genes
    nsv6137618copy number variation1nstd213human GRCh37 chrX: 52,510,000-58,560,001 , GRCh38.p12 chrX: 52,523,686-58,533,568 ACTG1P10, ALAS2, 106 more genes
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