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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5878993copy number variation1nstd209human GRCh38 chrX: 154,598,638-155,803,675 , GRCh37.p13 chrX|NW_003871103.3: 2,032,617-3,110,903 , GRCh37.p13 chrX: 153,826,899-154,906,585 MIR1184-2, TMLHE-AS1, 39 more genes
    nsv5728584mobile element insertion1nstd211human GRCh38 chrX: 154,849,478-154,849,478 , GRCh37.p13 chrX|NW_003871103.3: 2,283,457-2,283,457 , GRCh37.p13 chrX: 154,077,753-154,077,753 F8
    nsv5721929mobile element insertion2nstd211human GRCh38 chrX: 154,937,954-154,937,954 , GRCh37.p13 chrX: 154,166,229-154,166,229 , GRCh37.p13 chrX|NW_003871103.3: 2,371,933-2,371,933 F8
    nsv5717276mobile element insertion1nstd211human GRCh38 chrX: 154,839,751-154,839,751 , GRCh37.p13 chrX|NW_003871103.3: 2,273,730-2,273,730 , GRCh37.p13 chrX: 154,068,026-154,068,026 F8
    nsv5673836copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 154,159,808-154,166,711 , GRCh38 chrX: 154,931,533-154,938,436 F8
    nsv5560128mobile element insertion1nstd206human GRCh38 chrX: 154,937,954-154,938,005 , GRCh37.p13 chrX: 154,166,229-154,166,280 , GRCh37.p13 chrX|NW_003871103.3: 2,371,933-2,371,984 F8
    nsv5560081mobile element insertion1nstd206human GRCh38 chrX: 154,839,751-154,839,802 , GRCh37.p13 chrX: 154,068,026-154,068,077 , GRCh37.p13 chrX|NW_003871103.3: 2,273,730-2,273,781 F8
    nsv5433729copy number variation1nstd206human GRCh38 chrX: 154,834,121-154,835,442 , GRCh37.p13 chrX: 154,062,396-154,063,717 , GRCh37.p13 chrX|NW_003871103.3: 2,268,100-2,269,421 SMIM9, F8
    nsv5432979copy number variation1nstd206human GRCh37.p13 chrX|NW_003871103.3: 2,315,585-2,483,585 , GRCh38 chrX: 154,881,606-155,049,606 , GRCh37.p13 chrX: 154,109,881-154,277,881 F8, F8A1, 5 more genes
    nsv5424386copy number variation1nstd206human GRCh38 chrX: 154,838,529-154,838,635 , GRCh37.p13 chrX|NW_003871103.3: 2,272,508-2,272,614 , GRCh37.p13 chrX: 154,066,804-154,066,910 F8
    nsv5380366translocation1nstd200human GRCh38 chrX: 154,907,041-154,907,041 , GRCh38 chrX: 154,906,983-154,906,983 , GRCh37.p13 chrX: 154,135,258-154,135,258 , GRCh37.p13 chrX|NW_003871103.3: 2,341,020-2,341,020 , GRCh37.p13 chrX|NW_003871103.3: 2,340,962-2,340,962 , GRCh37.p13 chrX: 154,135,316-154,135,316 EEF1A1P31, F8
    nsv5200199mobile element insertion1nstd203human GRCh38 chrX: 154,989,284-154,989,299 , GRCh37.p13 chrX|NW_003871103.3: 2,423,263-2,423,278 , GRCh37.p13 chrX: 154,217,559-154,217,574 F8
    nsv5181491mobile element insertion1nstd203human GRCh38 chrX: 155,009,422-155,009,437 , GRCh37.p13 chrX|NW_003871103.3: 2,443,401-2,443,416 , GRCh37.p13 chrX: 154,237,697-154,237,712 F8
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4909295copy number variation1nstd200human GRCh38 chrX: 154,820,203-154,847,590 , GRCh37.p13 chrX|NW_003871103.3: 2,254,182-2,281,569 , GRCh37.p13 chrX: 154,048,478-154,075,865 SMIM9, F8
    nsv4909294copy number variation1nstd200human GRCh38 chrX: 154,810,407-155,540,834 , GRCh37.p13 chrX: 154,038,682-154,770,495 , GRCh37.p13 chrX|NW_003871103.3: 2,244,386-2,974,813 HMGN1P37, F8A3, 25 more genes
    nsv4894193copy number variation1nstd200human GRCh38 chrX: 154,879,755-154,880,688 , GRCh37.p13 chrX: 154,108,030-154,108,963 , GRCh37.p13 chrX|NW_003871103.3: 2,313,734-2,314,667 F8
    nsv4787995copy number variation1nstd200human GRCh37 chrX: 154,230,088-154,231,971 , GRCh38.p12 chrX: 155,001,813-155,003,696 F8
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