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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4415158copy number variation1nstd174human GRCh37 chr19: 988,772-989,511 , GRCh38.p12 chr19: 988,772-989,511 WDR18
    nsv4360507copy number variation1nstd102humanPathogenic NCBI36 chr19: 542,812-1,309,151 , GRCh37.p13 chr19: 591,812-1,358,151 , GRCh38.p12 chr19: 591,812-1,358,152 WDR18, GPX4, 52 more genes
    nsv4359760copy number variation1nstd102humanPathogenic NCBI36 chr19: 737,550-1,248,499 , GRCh37.p13 chr19: 786,550-1,297,499 , GRCh38.p12 chr19: 786,550-1,297,500 WDR18, CIRBP, 36 more genes
    nsv4358978copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-1,903,649 , GRCh37.p13 chr19: 259,395-1,952,649 , GRCh38.p12 chr19: 259,395-1,952,650 WDR18, ATP5F1D, 99 more genes
    nsv4358278copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37.p13 chr19: 233,565-4,699,484 , GRCh38.p12 chr19: 233,565-4,699,472 WDR18, TLE5, 216 more genes
    nsv4358092copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-6,746,622 , GRCh37.p13 chr19: 259,395-6,795,622 , GRCh38.p12 chr19: 259,395-6,795,611 WDR18, DAPK3, 286 more genes
    nsv4356943copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,019,506 , GRCh37.p13 chr19: 259,395-2,068,506 , GRCh38.p12 chr19: 259,395-2,068,507 WDR18, ARID3A, 102 more genes
    nsv4356047copy number variation1nstd102humanPathogenic NCBI36 chr19: 896,098-1,923,298 , GRCh37.p13 chr19: 945,098-1,972,298 , GRCh38.p12 chr19: 945,098-1,972,299 WDR18, POLR2E, 58 more genes
    nsv4356046copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,506,147 , GRCh37.p13 chr19: 259,395-2,555,147 , GRCh38.p12 chr19: 259,395-2,555,149 WDR18, AZU1, 129 more genes
    nsv4355738copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,195-1,302,362 , GRCh37.p13 chr19: 259,195-1,351,362 , GRCh38.p12 chr19: 259,195-1,351,363 WDR18, ATP5F1D, 66 more genes
    nsv4350974copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 372,537-2,848,919 , GRCh37.p13 chr19: 421,537-2,897,919 , GRCh38.p12 chr19: 421,537-2,897,921 WDR18, ATP5F1D, 135 more genes
    nsv4350779copy number variation1nstd102humanPathogenic GRCh37 chr19: 275,925-1,892,275 , GRCh38.p12 chr19: 275,925-1,892,276 WDR18, AZU1, 94 more genes
    nsv4350764copy number variation1nstd102humanPathogenic GRCh37 chr19: 839,492-995,557 , GRCh38.p12 chr19: 839,492-995,558 WDR18, ARID3A, 7 more genes
    nsv4326762insertion1nstd166human GRCh37.p13 chr19: 278,904-23,448,419 , GRCh38.p12 chr19: 278,904-23,265,617 WDR18, AMH, 1021 more genes
    nsv4270877copy number variation1nstd166human GRCh37.p13 chr19: 981,671-982,956 , GRCh38.p12 chr19: 981,671-982,956 WDR18
    nsv4265095copy number variation1nstd166human GRCh37.p13 chr19: 989,009-989,222 , GRCh38.p12 chr19: 989,009-989,222 WDR18
    nsv4263590copy number variation1nstd166human GRCh37.p13 chr19: 989,024-989,238 , GRCh38.p12 chr19: 989,024-989,238 WDR18
    nsv4259405copy number variation1nstd166human GRCh37.p13 chr19: 981,315-982,956 , GRCh38.p12 chr19: 981,315-982,956 WDR18
    nsv3961622copy number variation1nstd168human GRCh38 chr19: 940,995-1,014,341 , GRCh37.p13 chr19: 940,995-1,014,340 WDR18, GRIN3B, 3 more genes
    nsv3909324copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,200,875 , GRCh38.p12 chr19: 260,911-3,200,877 WDR18, AZU1, 153 more genes
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