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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957613insertion1nstd209human GRCh38 chr6: 30,254,208-30,254,208 , GRCh37.p13 chr6: 30,221,985-30,221,985 HCG17
    nsv5954685insertion1nstd209human GRCh38 chr6: 30,298,431-30,298,431 , GRCh37.p13 chr6: 30,266,208-30,266,208 HCG17, HCG18
    nsv5901654copy number variation1nstd209human GRCh38 chr6: 30,244,770-30,246,416 , GRCh37.p13 chr6: 30,212,547-30,214,193 HCG17
    nsv5900698copy number variation1nstd209human GRCh38 chr6: 30,318,665-30,319,097 , GRCh37.p13 chr6: 30,286,442-30,286,874 HCG18, HCG17
    nsv5891048copy number variation1nstd209human GRCh38 chr6: 30,240,031-30,240,449 , GRCh37.p13 chr6: 30,207,808-30,208,226 TRIM26BP, HCG17
    nsv5844600copy number variation1nstd209human GRCh38 chr6: 30,244,733-30,246,382 , GRCh37.p13 chr6: 30,212,510-30,214,159 HCG17
    nsv5715924mobile element insertion2nstd211human GRCh38 chr6: 30,320,086-30,320,086 , GRCh37.p13 chr6: 30,287,863-30,287,863 HCG18, HCG17
    nsv5688208mobile element insertion2nstd211human GRCh38 chr6: 30,279,438-30,279,438 , GRCh37.p13 chr6: 30,247,215-30,247,215 HCG17
    nsv5687223mobile element insertion1nstd211human GRCh38 chr6: 30,245,543-30,245,543 , GRCh37.p13 chr6: 30,213,320-30,213,320 HCG17
    nsv5683732mobile element insertion2nstd211human GRCh38 chr6: 30,254,220-30,254,220 , GRCh37.p13 chr6: 30,221,997-30,221,997 HCG17
    nsv5634441insertion1nstd207human GRCh38 chr6: 30,254,208-30,254,208 , GRCh37.p13 chr6: 30,221,985-30,221,985 HCG17
    nsv5576525copy number variation1nstd207human GRCh38 chr6: 30,262,742-30,262,813 , GRCh37.p13 chr6: 30,230,519-30,230,590 HLA-L, HCG17
    nsv5568357copy number variation1nstd207human GRCh38 chr6: 30,240,031-30,240,449 , GRCh37.p13 chr6: 30,207,808-30,208,226 HCG17, TRIM26BP
    nsv5560550mobile element insertion1nstd206human GRCh38 chr6: 30,320,102-30,320,137 , GRCh37.p13 chr6: 30,287,879-30,287,914 HCG17, HCG18
    nsv5543512insertion1nstd206human GRCh38 chr6: 30,254,208-30,254,208 , GRCh37.p13 chr6: 30,221,985-30,221,985 HCG17
    nsv5467977copy number variation1nstd206human GRCh38 chr6: 30,240,270-30,240,596 , GRCh37.p13 chr6: 30,208,047-30,208,373 HCG17, TRIM26BP
    nsv5388347copy number variation1nstd186human GRCh37 chr6: 30,207,864-30,208,182 , GRCh38.p12 chr6: 30,240,087-30,240,405 HCG17, TRIM26BP
    nsv5387169copy number variation1nstd186human GRCh37 chr6: 30,230,521-30,230,591 , GRCh38.p12 chr6: 30,262,744-30,262,814 HCG17, HLA-L
    nsv5385495copy number variation1nstd186human GRCh37 chr6: 30,207,681-30,208,063 , GRCh38.p12 chr6: 30,239,904-30,240,286 HCG17, TRIM26BP
    nsv5383754mobile element deletion1nstd186human GRCh37 chr6: 30,208,056-30,208,365 , GRCh38.p12 chr6: 30,240,279-30,240,588 TRIM26BP, HCG17
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