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Items: 1 to 20 of 307

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 more genes
    nsv5708518mobile element insertion1nstd211human GRCh38 chr18: 3,255,441-3,255,441 , GRCh37.p13 chr18: 3,255,439-3,255,439 MYL12A, MYL12-AS1
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5531364copy number variation1nstd206human GRCh38 chr18: 3,206,000-3,412,000 , GRCh37.p13 chr18: 3,205,998-3,411,998 MYOM1, TGIF1, 8 more genes
    nsv5433178mobile element insertion1nstd206human GRCh38 chr18: 3,255,441-3,255,492 , GRCh37.p13 chr18: 3,255,439-3,255,490 MYL12A, MYL12-AS1
    nsv5354200translocation1nstd200human GRCh38 chr10: 15,696,271-15,696,271 , GRCh38 chr18: 3,255,951-3,255,951 , GRCh37.p13 chr10: 15,738,270-15,738,270 , GRCh37.p13 chr18: 3,255,949-3,255,949 ITGA8, MYL12A, 1 more genes
    nsv5343889translocation1nstd200human GRCh37 chr10: 15,738,270-15,738,270 , GRCh37 chr18: 3,255,949-3,255,949 , GRCh38.p12 chr10: 15,696,271-15,696,271 , GRCh38.p12 chr18: 3,255,951-3,255,951 ITGA8, MYL12A, 1 more genes
    nsv5321644copy number variation1nstd204human GRCh38.p13 chr18: 2,770,369-3,867,276 , GRCh37.p13 chr18: 2,770,367-3,867,276 , MYL12B, 25 more genes
    nsv5299050copy number variation1nstd204human GRCh38.p13 chr18: 3,230,352-3,260,076 , GRCh37.p13 chr18: 3,230,350-3,260,074 MYL12-AS1, LOC101927044, 1 more genes
    nsv5294445copy number variation1nstd204human GRCh38.p13 chr18: 3,246,219-3,248,418 , GRCh37.p13 chr18: 3,246,217-3,248,416 LOC101927044, MYL12A
    nsv5286052copy number variation1nstd204human GRCh38.p13 chr18: 2,770,801-3,600,700 , GRCh37.p13 chr18: 2,770,799-3,600,698 LPIN2, LOC100419892, 22 more genes
    nsv5146001mobile element insertion1nstd203human GRCh38 chr18: 3,255,425-3,255,441 , GRCh37.p13 chr18: 3,255,423-3,255,439 MYL12A, MYL12-AS1
    nsv5014202copy number variation1nstd200human GRCh38 chr18: 3,096,086-3,385,261 , GRCh37.p13 chr18: 3,096,084-3,385,259 MYL12A, LOC101927044, 5 more genes
    nsv4867718copy number variation1nstd200human GRCh37 chr18: 3,245,810-3,246,996 , GRCh38.p12 chr18: 3,245,812-3,246,998 MYL12A, LOC101927044
    nsv4854494copy number variation1nstd200human GRCh37 chr18: 3,096,084-3,385,259 , GRCh38.p12 chr18: 3,096,086-3,385,261 MYOM1, LINC01895, 5 more genes
    nsv4854492copy number variation1nstd200human GRCh37 chr18: 2,770,703-3,867,127 , GRCh38.p12 chr18: 2,770,705-3,867,127 , SMCHD1, 25 more genes
    nsv4729860copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-3,415,478 , GRCh38.p12 chr18: 136,226-3,415,480 AIDAP3, LOC105371963, 56 more genes
    nsv4684364copy number variation1nstd102humanPathogenic GRCh37 chr18: 3,162,390-4,390,081 , GRCh38.p12 chr18: 3,162,392-4,390,081 MYOM1, TGIF1, 23 more genes
    nsv4679619copy number variation1nstd189human GRCh37.p13 chr18: 2,892,475-3,310,070 , GRCh38.p12 chr18: 2,892,477-3,310,072 MYOM1, LPIN2, 9 more genes
    nsv4676413copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-5,407,839 , GRCh38.p12 chr18: 136,226-5,407,840 CHORDC1P4, LOC105371958, 83 more genes
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