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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 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
    nsv5561441sequence alteration1nstd206human GRCh38 chr18: 3,794,039-6,839,596 , GRCh37.p13 chr18: 3,794,039-6,839,595 DLGAP1, LINC01387, 35 more genes
    nsv5375059translocation1nstd200human GRCh38 chr18: 5,291,746-5,291,746 , GRCh38 chr18: 3,134,944-3,134,944 , GRCh37.p13 chr18: 3,134,942-3,134,942 , GRCh37.p13 chr18: 5,291,745-5,291,745 ZBTB14, MYOM1
    nsv4676413copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-5,407,839 , GRCh38.p12 chr18: 136,226-5,407,840 CHORDC1P4, LOC105371958, 83 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
    nsv4676382copy number variation1nstd102humanPathogenic GRCh37 chr18: 544,117-5,679,224 , GRCh38.p12 chr18: 544,117-5,679,225 IGLJCOR18, CHORDC1P4, 79 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
    nsv4624909copy number variation1nstd183human GRCh37 chr18: 5,294,874-5,296,604 , GRCh38.p12 chr18: 5,294,875-5,296,605 ZBTB14
    nsv4619490copy number variation1nstd183human GRCh37 chr18: 5,208,906-5,321,715 , GRCh38.p12 chr18: 5,208,907-5,321,716 LOC107985144, LINC00526, 3 more genes
    nsv4532113copy number variation1nstd166human GRCh37.p13 chr18: 5,180,741-5,335,174 , GRCh38.p12 chr18: 5,180,742-5,335,175 ZBTB14, LINC00526, 4 more genes
    nsv4423855copy number variation1nstd174human GRCh37 chr18: 5,294,874-5,296,604 , GRCh38.p12 chr18: 5,294,875-5,296,605 ZBTB14
    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
    nsv3972375copy number variation1nstd102humanLikely benign GRCh37 chr18: 3,899,296-5,433,496 , GRCh38.p12 chr18: 3,899,296-5,433,497 ZBTB14, DLGAP1, 15 more genes
    nsv3963686copy number variation1nstd168human GRCh38 chr18: 5,286,732-5,344,483 , GRCh37.p13 chr18: 5,286,731-5,344,482 ZBTB14, LOC107985144
    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
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