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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5499261copy number variation1nstd206human GRCh38 chr11: 118,656,568-118,712,384 , GRCh37.p13 chr11|NW_003871072.2: 282,006-337,822 , GRCh37.p13 chr11: 118,527,278-118,583,093 RNU6-376P, PHLDB1, 3 more genes
    nsv4980933copy number variation1nstd200human GRCh38 chr11: 118,678,557-118,683,667 , GRCh37.p13 chr11|NW_003871072.2: 303,995-309,105 , GRCh37.p13 chr11: 118,549,266-118,554,376 TREH
    nsv4980932copy number variation1nstd200human GRCh38 chr11: 118,673,032-118,678,257 , GRCh37.p13 chr11|NW_003871072.2: 298,470-303,695 , GRCh37.p13 chr11: 118,543,741-118,548,966 TREH
    nsv4840487copy number variation1nstd200human GRCh37 chr11: 118,549,266-118,554,376 , GRCh38.p12 chr11: 118,678,557-118,683,667 TREH
    nsv4838148copy number variation1nstd200human GRCh37 chr11: 118,543,741-118,548,966 , GRCh38.p12 chr11: 118,673,032-118,678,257 TREH
    nsv4754312insertion1nstd199human GRCh37 chr11: 118,549,246-118,549,246 , GRCh38.p12 chr11: 118,678,537-118,678,537 TREH
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4683551copy number variation9nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 117,856,768-118,972,385 , GRCh38.p12 chr11: 117,986,053-119,101,675 MIR6716, TREHP1, 48 more genes
    nsv4675236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396 SETP16, UPK2, 59 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4617347copy number variation1nstd183human GRCh37 chr11: 118,532,388-118,532,432 , GRCh38.p12 chr11: 118,661,679-118,661,723 TREH
    nsv4614121copy number variation1nstd183human GRCh37 chr11: 118,550,756-118,556,894 , GRCh38.p12 chr11: 118,680,047-118,686,185 TREH, TREHP1
    nsv4599777copy number variation1nstd183human GRCh37 chr11: 118,549,154-118,562,068 , GRCh38.p12 chr11: 118,678,445-118,691,359 TREHP1, TREH, 1 more genes
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
    nsv4451218copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,007,722-119,170,511 , GRCh38.p12 chr11: 118,137,007-119,299,801 ABCG4, CCDC153, 52 more genes
    nsv4377454copy number variation1nstd173human GRCh37 chr11: 118,355,769-118,621,008 , GRCh38.p12 chr11: 118,485,054-118,750,298 PHLDB1, IFT46, 13 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4207149copy number variation1nstd166human GRCh37.p13 chr11: 118,549,362-118,554,423 , GRCh38.p12 chr11: 118,678,653-118,683,714 TREH
    nsv4202412copy number variation1nstd166human GRCh37.p13 chr11: 118,543,742-118,548,968 , GRCh38.p12 chr11: 118,673,033-118,678,259 TREH
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