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Items: 1 to 20 of 241

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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
    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
    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
    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
    nsv4676141copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617 ANKRD12, DLGAP1-AS1, 270 more genes
    nsv4676139copy number variation1nstd102humanUncertain significance GRCh37 chr18: 8,165,369-9,557,565 , GRCh38.p12 chr18: 8,165,371-9,557,567 RNU2-27P, RN7SL50P, 19 more genes
    nsv4628265copy number variation1nstd183human GRCh37 chr18: 9,124,817-9,125,104 , GRCh38.p12 chr18: 9,124,819-9,125,106 NDUFV2-AS1, NDUFV2
    nsv4619100copy number variation1nstd183human GRCh37 chr18: 9,098,969-9,150,628 , GRCh38.p12 chr18: 9,098,971-9,150,630 NDUFV2, ANKRD12, 1 more genes
    nsv4457714copy number variation1nstd102humanUncertain significance GRCh37 chr18: 7,188,753-9,408,889 , GRCh38.p12 chr18: 7,188,755-9,408,891 GACAT2, RAB12, 22 more genes
    nsv4385858copy number variation1nstd173human GRCh37 chr18: 136,227-18,529,578 , GRCh38.p12 chr18: 136,227-20,949,617 , LOC105371995, 276 more genes
    nsv4366605copy number variation1nstd173human GRCh37 chr18: 9,065,458-9,142,999 , GRCh38.p12 chr18: 9,065,460-9,143,001 NDUFV2-AS1, ANKRD12, 1 more genes
    nsv4348774copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-15,175,005 , GRCh38.p12 chr18: 136,226-15,175,006 ANKRD62, LOC100419892, 263 more genes
    nsv4256683copy number variation1nstd166human GRCh37.p13 chr18: 9,116,016-9,163,793 , GRCh38.p12 chr18: 9,116,018-9,163,795 NDUFV2-AS1, ANKRD12, 1 more genes
    nsv3924832copy number variation1nstd102humanPathogenic NCBI36 chr18: 4,275-12,801,387 , GRCh37.p13 chr18: 14,275-12,811,387 , GRCh38.p12 chr18: 14,275-12,811,388 PIEZO2, LINC01882, 211 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924580copy number variation1nstd102humanPathogenic GRCh38 chr18: 118,760-15,024,003 , GRCh37 chr18: 118,760-15,024,002 , NCBI36 chr18: 108,760-15,014,002 LOC105371951, GAPDHP66, 264 more genes
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