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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7038170inversion1nstd229human GRCh38 chr2: 119,747,881-120,301,832 , GRCh37.p13 chr2: 120,505,457-121,059,408 RPL27P7, MTND5P28, 12 more genes
    nsv6696497copy number variation1nstd229human GRCh38 chr2: 120,227,277-120,275,270 , GRCh37.p13 chr2: 120,984,853-121,032,846 LOC105373583, RALB
    nsv6694258copy number variation1nstd229human GRCh38 chr2: 120,215,301-120,582,100 , GRCh37.p13 chr2: 120,972,877-121,339,676 INHBB, LOC105373585, 8 more genes
    nsv6690988copy number variation1nstd229human GRCh38 chr2: 120,260,332-120,264,499 , GRCh37.p13 chr2: 121,017,908-121,022,075 RALB
    nsv6684246copy number variation1nstd229human GRCh38 chr2: 120,287,068-120,296,285 , GRCh37.p13 chr2: 121,044,644-121,053,861 RALB
    nsv6683231copy number variation1nstd229human GRCh38 chr2: 120,263,801-120,269,200 , GRCh37.p13 chr2: 121,021,377-121,026,776 RALB
    nsv6636914copy number variation1nstd102humanUncertain significance GRCh37 chr2: 120,729,215-121,383,896 , GRCh38.p12 chr2: 119,971,639-120,626,320 MTND4P26, EPB41L5, 16 more genes
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6353100copy number variation1nstd223human GRCh38 chr2: 120,260,332-120,264,498 , GRCh37.p13 chr2: 121,017,908-121,022,074 RALB
    nsv6350536copy number variation1nstd223human GRCh38 chr2: 120,276,401-120,279,700 , GRCh37.p13 chr2: 121,033,977-121,037,276 RALB
    nsv6338999copy number variation1nstd223human GRCh38 chr2: 120,276,636-120,282,763 , GRCh37.p13 chr2: 121,034,212-121,040,339 RALB
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315168copy number variation1nstd102humanPathogenic GRCh37 chr2: 120,628,484-127,658,188 , GRCh38.p12 chr2: 119,870,908-126,900,612 TSN, LOC107985817, 58 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6290805copy number variation1nstd102humanUncertain significance GRCh37 chr2: 119,967,365-121,555,029 , GRCh38.p12 chr2: 119,209,789-120,797,453 LOC101927764, MTND5P28, 29 more genes
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