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Items: 1 to 20 of 932

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4348503copy number variation1nstd102humanPathogenic GRCh37 chrX: 147,642,893-147,870,805 , GRCh38.p12 chrX: 148,561,372-148,789,281 AFF2
    nsv3881796copy number variation1nstd102humanPathogenic GRCh37 chrX: 147,573,612-147,620,560 , GRCh38.p12 chrX: 148,492,092-148,539,039 AFF2
    nsv6313800copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 147,573,781-147,628,228 , GRCh38.p12 chrX: 148,492,261-148,546,707 AFF2
    nsv3893697copy number variation1nstd102humanUncertain significance GRCh38 chrX: 148,959,372-149,023,968 , NCBI36 chrX: 147,848,598-147,913,208 , GRCh37 chrX: 148,040,902-148,105,498 AFF2
    nsv3896334copy number variation1nstd102humanUncertain significance GRCh38 chrX: 148,999,676-149,003,587 , GRCh37.p13 chrX|NW_004070890.2: 4,524,073-4,527,984 , NCBI36 chrX: 147,888,912-147,892,823 AFF2
    nsv3881416copy number variation1nstd102humanUncertain significance GRCh37 chrX: 148,050,494-148,155,055 , GRCh38.p12 chrX: 148,968,964-149,073,525 AFF2
    nsv3871986copy number variation1nstd102humanUncertain significance GRCh37 chrX: 147,579,427-147,603,852 , GRCh38.p12 chrX: 148,497,907-148,522,331 AFF2
    nsv7085268copy number variation1nstd229human GRCh38 chrX: 148,588,201-148,638,900 , GRCh37.p13 chrX: 147,669,722-147,720,421 , GRCh37.p13 chrX|NW_004070890.2: 4,112,595-4,163,294 AFF2
    nsv7085293copy number variation1nstd229human GRCh38 chrX: 148,849,401-148,898,800 , GRCh37.p13 chrX|NW_004070890.2: 4,373,798-4,423,197 , GRCh37.p13 chrX: 147,930,930-147,980,330 AFF2
    nsv7085269copy number variation1nstd229human GRCh38 chrX: 148,595,501-148,638,900 , GRCh37.p13 chrX: 147,677,022-147,720,421 , GRCh37.p13 chrX|NW_004070890.2: 4,119,895-4,163,294 AFF2
    nsv7085278copy number variation1nstd229human GRCh38 chrX: 148,687,671-148,729,686 , GRCh37.p13 chrX: 147,769,195-147,811,210 , GRCh37.p13 chrX|NW_004070890.2: 4,212,068-4,254,083 AFF2
    nsv7085274copy number variation1nstd229human GRCh38 chrX: 148,666,947-148,706,347 , GRCh37.p13 chrX: 147,748,468-147,787,871 , GRCh37.p13 chrX|NW_004070890.2: 4,191,341-4,230,744 AFF2
    nsv7085271copy number variation1nstd229human GRCh38 chrX: 148,602,601-148,638,900 , GRCh37.p13 chrX: 147,684,122-147,720,421 , GRCh37.p13 chrX|NW_004070890.2: 4,126,995-4,163,294 AFF2
    nsv7085270copy number variation1nstd229human GRCh38 chrX: 148,599,201-148,629,200 , GRCh37.p13 chrX|NW_004070890.2: 4,123,595-4,153,594 , GRCh37.p13 chrX: 147,680,722-147,710,721 AFF2
    nsv7085264copy number variation1nstd229human GRCh38 chrX: 148,571,235-148,595,585 , GRCh37.p13 chrX|NW_004070890.2: 4,095,629-4,119,979 , GRCh37.p13 chrX: 147,652,756-147,677,106 AFF2
    nsv7085280copy number variation1nstd229human GRCh38 chrX: 148,715,749-148,736,011 , GRCh37.p13 chrX|NW_004070890.2: 4,240,146-4,260,408 , GRCh37.p13 chrX: 147,797,273-147,817,535 AFF2
    nsv7085295copy number variation1nstd229human GRCh38 chrX: 148,889,501-148,902,500 , GRCh37.p13 chrX|NW_004070890.2: 4,413,898-4,426,897 , GRCh37.p13 chrX: 147,971,031-147,984,030 AFF2
    nsv7085292copy number variation1nstd229human GRCh38 chrX: 148,849,401-148,860,900 , GRCh37.p13 chrX|NW_004070890.2: 4,373,798-4,385,297 , GRCh37.p13 chrX: 147,930,930-147,942,430 AFF2
    nsv7085291copy number variation1nstd229human GRCh38 chrX: 148,849,401-148,860,000 , GRCh37.p13 chrX|NW_004070890.2: 4,373,798-4,384,397 , GRCh37.p13 chrX: 147,930,930-147,941,530 AFF2
    nsv7085262copy number variation1nstd229human GRCh38 chrX: 148,549,201-148,559,300 , GRCh37.p13 chrX|NW_004070890.2: 4,073,595-4,083,694 , GRCh37.p13 chrX: 147,630,722-147,640,821 AFF2
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