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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7072608inversion1nstd229human GRCh38 chr19: 38,415,065-38,418,338 , GRCh37.p13 chr19: 38,905,705-38,908,978 RASGRP4
    nsv7017337copy number variation1nstd229human GRCh38 chr19: 38,396,742-38,612,341 , GRCh37.p13 chr19: 38,887,382-39,102,981 SPRED3, MAP4K1, 4 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6599122inversion1nstd223human GRCh38 chr19: 38,415,064-38,418,338 , GRCh37.p13 chr19: 38,905,704-38,908,978 RASGRP4
    nsv6531255copy number variation1nstd223human GRCh38 chr19: 38,415,064-38,422,101 , GRCh37.p13 chr19: 38,905,704-38,912,741 RASGRP4
    nsv6528802copy number variation1nstd223human GRCh38 chr19: 37,602,649-38,484,499 , GRCh37.p13 chr19: 38,093,550-38,975,139 SPRED3, PSMD8, 30 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6102141insertion1nstd212human GRCh38 chr19: 38,407,938-38,407,938 , GRCh37.p13 chr19: 38,898,578-38,898,578 FAM98C, RASGRP4
    nsv5556604sequence alteration1nstd206human GRCh38 chr19: 38,269,810-38,604,627 , GRCh37.p13 chr19: 38,760,450-39,095,267 , PSMD8, 12 more genes
    nsv5027879copy number variation1nstd200human GRCh38 chr19: 38,415,037-38,422,128 , GRCh37.p13 chr19: 38,905,677-38,912,768 RASGRP4
    nsv5027878copy number variation1nstd200human GRCh38 chr19: 38,408,209-38,408,372 , GRCh37.p13 chr19: 38,898,849-38,899,012 RASGRP4, FAM98C
    nsv4676223copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,512,717-39,291,526 , GRCh38.p12 chr19: 38,022,077-38,800,886 MAP4K1-AS1, LGALS7B, 25 more genes
    nsv4620427copy number variation1nstd183human GRCh37 chr19: 38,903,099-38,921,117 , GRCh38.p12 chr19: 38,412,459-38,430,477 RASGRP4
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4271135copy number variation1nstd166human GRCh37.p13 chr19: 38,900,636-38,900,728 , GRCh38.p12 chr19: 38,409,996-38,410,088 RASGRP4
    nsv4254152copy number variation1nstd166human GRCh37.p13 chr19: 38,888,986-38,901,189 , GRCh38.p12 chr19: 38,398,346-38,410,549 RASGRP4, SPRED3, 1 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
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