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Items: 1 to 20 of 254

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940337copy number variation1nstd209human GRCh38 chr18: 10,530,068-10,530,123 , GRCh37.p13 chr18: 10,530,065-10,530,120 NAPG
    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
    nsv4854538copy number variation1nstd200human GRCh37 chr18: 10,379,246-10,533,406 , GRCh38.p12 chr18: 10,379,249-10,533,409 LOC105371988, APCDD1, 3 more genes
    nsv4730028copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,025,171-11,295,845 , GRCh38.p12 chr18: 10,025,174-11,295,846 KIAA0895LP1, NAPG, 15 more genes
    nsv4730023copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,261,224-10,539,806 , GRCh38.p12 chr18: 10,261,227-10,539,809 LINC01254, LOC105371988, 5 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
    nsv4684313copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,140,629-12,236,187 , GRCh38.p12 chr18: 10,140,632-12,236,188 PIEZO2, LOC105371986, 38 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
    nsv4634192copy number variation1nstd183human GRCh37 chr18: 10,532,529-10,533,681 , GRCh38.p12 chr18: 10,532,532-10,533,684 NAPG
    nsv4630864copy number variation1nstd183human GRCh37 chr18: 10,146,930-10,610,381 , GRCh38.p12 chr18: 10,146,933-10,610,384 , NAPG, 7 more genes
    nsv4630396copy number variation1nstd183human GRCh37 chr18: 10,468,310-10,603,620 , GRCh38.p12 chr18: 10,468,313-10,603,623 , APCDD1, 1 more genes
    nsv4623200copy number variation1nstd183human GRCh37 chr18: 10,466,001-10,596,012 , GRCh38.p12 chr18: 10,466,004-10,596,015 , APCDD1, 1 more genes
    nsv4620990copy number variation1nstd183human GRCh37 chr18: 10,532,591-10,532,844 , GRCh38.p12 chr18: 10,532,594-10,532,847 NAPG
    nsv4457878copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,466,856-10,597,678 , GRCh38.p12 chr18: 10,466,859-10,597,681 NAPG, APCDD1
    nsv4385858copy number variation1nstd173human GRCh37 chr18: 136,227-18,529,578 , GRCh38.p12 chr18: 136,227-20,949,617 , LOC105371995, 276 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
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