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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128404insertion1nstd186human GRCh37 chr4: 120,055,458-120,055,466 , GRCh38.p12 chr4: 119,134,303-119,134,311 MYOZ2
    nsv5964567insertion1nstd209human GRCh38 chr4: 119,150,496-119,150,496 , GRCh37.p13 chr4: 120,071,651-120,071,651 MYOZ2, LOC105379404
    nsv5892116copy number variation1nstd209human GRCh38 chr4: 119,134,256-119,134,306 , GRCh37.p13 chr4: 120,055,411-120,055,461 MYOZ2
    nsv5890853copy number variation1nstd209human GRCh38 chr4: 119,163,838-119,164,076 , GRCh37.p13 chr4: 120,084,993-120,085,231 MYOZ2
    nsv5692645mobile element insertion2nstd211human GRCh38 chr4: 119,150,512-119,150,512 , GRCh37.p13 chr4: 120,071,667-120,071,667 MYOZ2, LOC105379404
    nsv5621900insertion1nstd207human GRCh38 chr4: 119,150,496-119,150,496 , GRCh37.p13 chr4: 120,071,651-120,071,651 LOC105379404, MYOZ2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5541153insertion1nstd206human GRCh38 chr4: 119,134,299-119,134,307 , GRCh37.p13 chr4: 120,055,454-120,055,462 MYOZ2
    nsv5538289insertion1nstd206human GRCh38 chr4: 119,134,303-119,134,311 , GRCh37.p13 chr4: 120,055,458-120,055,466 MYOZ2
    nsv5538086insertion1nstd206human GRCh38 chr4: 119,134,202-119,134,252 , GRCh37.p13 chr4: 120,055,357-120,055,407 MYOZ2
    nsv5473479copy number variation1nstd206human GRCh38 chr4: 119,137,928-119,139,859 , GRCh37.p13 chr4: 120,059,083-120,061,014 MYOZ2
    nsv5466206copy number variation1nstd206human GRCh38 chr4: 119,085,985-119,196,844 , GRCh37.p13 chr4: 120,007,140-120,117,999 MYOZ2, MRPL42P1, 4 more genes
    nsv5465471copy number variation1nstd206human GRCh38 chr4: 119,163,840-119,164,077 , GRCh37.p13 chr4: 120,084,995-120,085,232 MYOZ2
    nsv5458828copy number variation1nstd206human GRCh38 chr4: 119,137,718-119,137,768 , GRCh37.p13 chr4: 120,058,873-120,058,923 MYOZ2
    nsv5395933mobile element insertion1nstd206human GRCh38 chr4: 119,150,512-119,150,563 , GRCh37.p13 chr4: 120,071,667-120,071,718 LOC105379404, MYOZ2
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5381502copy number variation1nstd102humanUncertain significance GRCh37 chr4: 120,057,671-120,057,766 , GRCh38.p12 chr4: 119,136,516-119,136,611 MYOZ2
    nsv5093110mobile element insertion1nstd203human GRCh38 chr4: 119,150,501-119,150,512 , GRCh37.p13 chr4: 120,071,656-120,071,667 MYOZ2, LOC105379404
    nsv5091396mobile element insertion1nstd203human GRCh38 chr4: 119,150,498-119,150,512 , GRCh37.p13 chr4: 120,071,653-120,071,667 MYOZ2, LOC105379404
    nsv5091037mobile element insertion1nstd203human GRCh38 chr4: 119,150,503-119,150,512 , GRCh37.p13 chr4: 120,071,658-120,071,667 MYOZ2, LOC105379404
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