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Items: 1 to 20 of 394

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117672copy number variation1nstd186human GRCh37 chrX: 149,751,737-149,752,409 , GRCh38.p12 chrX: 150,583,277-150,583,949 MTM1
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5966868insertion1nstd209human GRCh38 chrX: 150,583,891-150,583,891 , GRCh37.p13 chrX|NW_004070890.2: 6,108,289-6,108,289 , GRCh37.p13 chrX: 149,752,351-149,752,351 MTM1
    nsv5887342copy number variation1nstd209human GRCh38 chrX: 150,583,397-150,583,926 , GRCh37.p13 chrX|NW_004070890.2: 6,107,795-6,108,324 , GRCh37.p13 chrX: 149,751,857-149,752,386 MTM1
    nsv5882231copy number variation1nstd209human GRCh38 chrX: 150,583,458-150,583,875 , GRCh37.p13 chrX|NW_004070890.2: 6,107,856-6,108,273 , GRCh37.p13 chrX: 149,751,918-149,752,335 MTM1
    nsv5729860mobile element insertion1nstd211human GRCh38 chrX: 150,626,752-150,626,752 , GRCh37.p13 chrX: 149,795,225-149,795,225 , GRCh37.p13 chrX|NW_004070890.2: 6,151,150-6,151,150 MTM1
    nsv5669474copy number variation1nstd207human GRCh37.p13 chrX|NW_004070890.2: 6,107,744-6,107,891 , GRCh38 chrX: 150,583,346-150,583,493 , GRCh37.p13 chrX: 149,751,806-149,751,953 MTM1
    nsv5668415copy number variation1nstd207human GRCh37.p13 chrX|NW_004070890.2: 6,107,939-6,108,346 , GRCh38 chrX: 150,583,541-150,583,948 , GRCh37.p13 chrX: 149,752,001-149,752,408 MTM1
    nsv5431445copy number variation1nstd206human GRCh38 chrX: 150,612,482-150,612,657 , GRCh37.p13 chrX: 149,780,955-149,781,130 , GRCh37.p13 chrX|NW_004070890.2: 6,136,880-6,137,055 MTM1
    nsv5429049copy number variation1nstd206human GRCh38 chrX: 150,604,237-150,604,296 , GRCh37.p13 chrX|NW_004070890.2: 6,128,635-6,128,694 , GRCh37.p13 chrX: 149,772,701-149,772,760 MTM1
    nsv5425959copy number variation1nstd206human GRCh38 chrX: 150,583,277-150,583,949 , GRCh37.p13 chrX|NW_004070890.2: 6,107,675-6,108,347 , GRCh37.p13 chrX: 149,751,737-149,752,409 MTM1
    nsv5425410copy number variation1nstd206human GRCh38 chrX: 150,623,595-150,623,661 , GRCh37.p13 chrX|NW_004070890.2: 6,147,993-6,148,059 , GRCh37.p13 chrX: 149,792,068-149,792,134 MTM1
    nsv5419428copy number variation1nstd206human GRCh38 chrX: 150,612,475-150,612,665 , GRCh37.p13 chrX: 149,780,948-149,781,138 , GRCh37.p13 chrX|NW_004070890.2: 6,136,873-6,137,063 MTM1
    nsv5380329translocation1nstd200human GRCh38 chrX: 150,572,933-150,572,933 , GRCh38 chrX: 150,572,984-150,572,984 , GRCh37.p13 chrX|NW_004070890.2: 6,097,331-6,097,331 , GRCh37.p13 chrX|NW_004070890.2: 6,097,382-6,097,382 , GRCh37.p13 chrX: 149,741,383-149,741,383 , GRCh37.p13 chrX: 149,741,434-149,741,434 MTM1
    nsv5200124mobile element insertion1nstd203human GRCh38 chrX: 150,629,505-150,629,519 , GRCh37.p13 chrX: 149,797,978-149,797,992 , GRCh37.p13 chrX|NW_004070890.2: 6,153,903-6,153,917 MTM1
    nsv5200123mobile element insertion1nstd203human GRCh38 chrX: 150,567,904-150,567,920 , GRCh37.p13 chrX|NW_004070890.2: 6,092,302-6,092,318 , GRCh37.p13 chrX: 149,736,354-149,736,370 MTM1
    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
    nsv4909265copy number variation1nstd200human GRCh38 chrX: 150,318,821-150,644,075 , GRCh37.p13 chrX: 149,487,057-149,812,548 , GRCh37.p13 chrX|NW_004070890.2: 5,843,219-6,168,473 MAMLD1, MTM1
    nsv4894154copy number variation1nstd200human GRCh38 chrX: 150,623,735-150,625,441 , GRCh37.p13 chrX|NW_004070890.2: 6,148,133-6,149,839 , GRCh37.p13 chrX: 149,792,208-149,793,914 MTM1
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
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