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Items: 1 to 20 of 27

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309294copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,574,771-95,598,850 , GRCh38.p12 chr11: 95,841,607-95,865,686 MTMR2
    nsv7094117copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,568,444-95,568,625 , GRCh38.p12 chr11: 95,835,280-95,835,461 MTMR2
    nsv6309390copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 95,568,454-95,598,860 , GRCh38.p12 chr11: 95,835,290-95,865,696 MTMR2, RNA5SP345
    nsv6309456copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,568,454-95,657,118 , GRCh38.p12 chr11: 95,835,290-95,923,954 MTMR2, RNA5SP345
    nsv7094116copy number variation1nstd102humanPathogenic GRCh37 chr11: 95,523,863-95,564,420 , GRCh38.p12 chr11: 95,790,699-95,831,256 MTMR2, CEP57, 1 more genes
    nsv6309241copy number variation1nstd102humanUncertain significance GRCh37 chr11: 95,523,863-95,569,448 , GRCh38.p12 chr11: 95,790,699-95,836,284 MTMR2, CEP57, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 MTMR2, FAUP4, 2031 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 MTMR2, RPS6P16, 449 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 MTMR2, PLS1P1, 349 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 MTMR2, PHB1P16, 385 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 MTMR2, LOC107984375, 295 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 MTMR2, LOC105369441, 296 more genes
    nsv3894488copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924 MTMR2, RNU6-16P, 270 more genes
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTMR2, MTND5P38, 252 more genes
    nsv3910663copy number variation1nstd102humanPathogenic GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308 MTMR2, LOC101060084, 230 more genes
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 MTMR2, AMOTL1, 240 more genes
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 MTMR2, HSPD1P13, 239 more genes
    nsv3897292copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057 MTMR2, FAM181B, 218 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 MTMR2, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 MTMR2, RTN3, 2833 more genes
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