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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5972218copy number variation2nstd209human GRCh38 chrX: 152,765,605-152,767,383 , GRCh37.p13 chrX: 151,869,578-151,871,356 , GRCh37.p13 chrX|NW_003871103.3: 199,588-201,366 MAGEA6
    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
    nsv4909276copy number variation1nstd200human GRCh38 chrX: 152,665,874-152,960,330 , GRCh37.p13 chrX: 151,834,345-152,128,874 , GRCh37.p13 chrX|NW_003871103.3: 99,857-394,313 LOC100420250, CSAG1, 15 more genes
    nsv4782435copy number variation1nstd200human GRCh37 chrX: 151,846,283-152,007,363 , GRCh38.p12 chrX: 152,677,823-152,838,819 MAGEA6-DT, CSAG2, 13 more genes
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4730087inversion22nstd198human GRCh37.p13 chrX: 151,856,022-151,934,375 , GRCh38 chrX: 152,702,624-152,780,919 , GRCh37.p13 chrX|NW_003871103.3: 136,607-214,902 MAGEA2, MAGEA3, 8 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4685620copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551 ABCD1, AMD1P2, 560 more genes
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4674080copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,387,417-155,233,731 , GRCh38.p12 chrX: 85,132,411-156,004,066 CSTF2, GPR119, 1029 more genes
    nsv4578241copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,757,437-155,208,244 , GRCh38.p12 chrX: 123,623,586-155,978,579 ABCD1, AMD1P2, 557 more genes
    nsv4454214copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,924,044-155,233,731 , GRCh38.p12 chrX: 123,790,194-156,004,066 LOC107985666, FLNA, 555 more genes
    nsv4452492copy number variation1nstd102humanPathogenic GRCh37 chrX: 58,455,352-155,233,731 , GRCh38.p12 chrX: 58,428,919-156,004,066 RNU6-122P, LOC100421910, 1347 more genes
    nsv4452442copy number variation1nstd102humanPathogenic GRCh37 chrX: 92,814,516-155,233,731 , GRCh38.p12 chrX: 93,559,517-156,004,066 TEX13D, CT45A5, 978 more genes
    nsv4451828copy number variation1nstd102humanPathogenic GRCh37 chrX: 118,150,047-155,233,731 , GRCh38.p12 chrX: 119,016,084-156,004,066 TFDP3, UBE2NL, 643 more genes
    nsv4450737copy number variation1nstd102humanPathogenic GRCh37 chrX: 104,098,124-155,233,731 , GRCh38.p12 chrX: 104,853,444-156,004,066 LOC107985699, IKBKGP1, 804 more genes
    nsv4450523copy number variation1nstd102humanUncertain significance GRCh37 chrX: 54,941,868-155,233,731 , GRCh38.p12 chrX: 54,915,435-156,004,066 LOC105373348, MIR548AN, 1396 more genes
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