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Items: 1 to 20 of 302

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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
    nsv5887334copy number variation1nstd209human GRCh38 chrX: 119,471,365-121,073,821 , GRCh37.p13 chrX: 118,605,328-120,207,675 , LOC105373328, 56 more genes
    nsv5669380copy number variation1nstd207human GRCh38 chrX: 120,876,168-120,976,282 , GRCh37.p13 chrX: 120,010,022-120,110,136 CT47A9, CT47A2, 10 more genes
    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
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 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
    nsv4728692copy number variation1nstd102humanPathogenic GRCh37 chrX: 117,120,780-129,850,994 , GRCh38.p12 chrX: 117,986,817-130,717,020 LOC107985709, SLC25A5, 171 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 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
    nsv4679893copy number variation1nstd189human GRCh37.p13 chrX: 113,759,648-150,222,670 , GRCh38.p12 chrX: 114,525,195-151,054,198 , AGTR2, 532 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
    nsv4673891copy number variation1nstd102humanPathogenic GRCh37 chrX: 117,119,895-129,850,963 , GRCh38.p12 chrX: 117,985,932-130,716,989 CT47A2, HSPA8P1, 171 more genes
    nsv4648304copy number variation1nstd186human GRCh37 chrX: 120,063,235-120,090,000 , GRCh38.p12 chrX: 120,929,382-120,956,146 CT47A11, CT47A7, 4 more genes
    nsv4633532copy number variation1nstd183human GRCh37 chrX: 120,067,471-120,120,958 , GRCh38.p12 chrX: 120,933,617-120,987,104 CT47A5, CT47A4, 9 more genes
    nsv4620452copy number variation2nstd183human GRCh37 chrX: 120,005,568-120,122,030 , GRCh38.p12 chrX: 120,871,714-120,988,176 CT47A12, CT47A7, 11 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
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