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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943835copy number variation1nstd209human GRCh38 chr18: 8,888,335-9,169,886 , GRCh37.p13 chr18: 8,888,333-9,169,884 NDUFV2, ANKRD12, 2 more genes
    nsv5940682copy number variation1nstd209human GRCh38 chr18: 9,111,498-9,112,087 , GRCh37.p13 chr18: 9,111,496-9,112,085 NDUFV2
    nsv5711085mobile element insertion1nstd211human GRCh38 chr18: 9,110,356-9,110,356 , GRCh37.p13 chr18: 9,110,354-9,110,354 NDUFV2
    nsv5696892mobile element insertion1nstd211human GRCh38 chr18: 9,114,252-9,114,252 , GRCh37.p13 chr18: 9,114,250-9,114,250 NDUFV2
    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
    nsv5527130copy number variation1nstd206human GRCh38 chr18: 9,111,209-9,112,088 , GRCh37.p13 chr18: 9,111,207-9,112,086 NDUFV2
    nsv5428363mobile element insertion1nstd206human GRCh38 chr18: 9,114,252-9,114,303 , GRCh37.p13 chr18: 9,114,250-9,114,301 NDUFV2
    nsv5392986copy number variation1nstd186human GRCh37 chr18: 9,111,549-9,112,085 , GRCh38.p12 chr18: 9,111,551-9,112,087 NDUFV2
    nsv5322069copy number variation1nstd204human GRCh38.p13 chr18: 9,111,522-9,112,116 , GRCh37.p13 chr18: 9,111,520-9,112,114 NDUFV2
    nsv5017594copy number variation1nstd200human GRCh38 chr18: 9,111,726-9,112,736 , GRCh37.p13 chr18: 9,111,724-9,112,734 NDUFV2
    nsv5017593copy number variation1nstd200human GRCh38 chr18: 9,103,745-9,103,827 , GRCh37.p13 chr18: 9,103,743-9,103,825 NDUFV2
    nsv5017592copy number variation1nstd200human GRCh38 chr18: 9,101,818-9,111,764 , GRCh37.p13 chr18: 9,101,816-9,111,762 NDUFV2
    nsv5014264copy number variation1nstd200human GRCh38 chr18: 9,072,044-9,143,791 , GRCh37.p13 chr18: 9,072,042-9,143,789 ANKRD12, NDUFV2-AS1, 1 more genes
    nsv4852012copy number variation1nstd200human GRCh37 chr18: 9,111,478-9,112,169 , GRCh38.p12 chr18: 9,111,480-9,112,171 NDUFV2
    nsv4852011copy number variation1nstd200human GRCh37 chr18: 9,101,816-9,111,762 , GRCh38.p12 chr18: 9,101,818-9,111,764 NDUFV2
    nsv4729915copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,598,173-15,422,644 , GRCh38.p12 chr18: 7,598,175-15,410,899 CEP192, RNU2-27P, 155 more genes
    nsv4676396copy number variation1nstd102humanPathogenic GRCh37 chr18: 971,295-11,250,447 , GRCh38.p12 chr18: 971,294-11,250,448 LOC100129774, LOC100419892, 146 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PRELID3A, ANKRD30B, 275 more genes
    nsv4676314copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715 EIF4A2P1, PMM2P2, 263 more genes
    nsv4676159copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-13,894,429 , GRCh38.p12 chr18: 136,226-13,894,430 SLC25A51P2, BOLA2P1, 221 more genes
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