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Items: 1 to 20 of 248

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098872copy number variation1nstd102humanUncertain significance GRCh37 chr2: 73,716,761-75,347,894 , GRCh38.p12 chr2: 73,489,634-75,120,768 RTKN, PCGF1, 61 more genes
    nsv7057254inversion1nstd229human GRCh38 chr2: 74,561,967-74,562,646 , GRCh37.p13 chr2: 74,789,094-74,789,773 M1AP
    nsv7039989inversion1nstd229human GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982 WBP1, DCTN1-AS1, 80 more genes
    nsv6697570copy number variation1nstd229human GRCh38 chr2: 74,645,014-74,781,337 , GRCh37.p13 chr2: 74,872,141-75,008,464 M1AP, SEMA4F, 3 more genes
    nsv6697501copy number variation1nstd229human GRCh38 chr2: 74,628,601-74,630,900 , GRCh37.p13 chr2: 74,855,728-74,858,027 M1AP, TVP23BP2
    nsv6695373copy number variation1nstd229human GRCh38 chr2: 74,605,832-74,607,648 , GRCh37.p13 chr2: 74,832,959-74,834,775 M1AP
    nsv6694127copy number variation1nstd229human GRCh38 chr2: 74,632,723-74,643,078 , GRCh37.p13 chr2: 74,859,850-74,870,205 M1AP
    nsv6693587copy number variation1nstd229human GRCh38 chr2: 74,598,755-74,998,174 , GRCh37.p13 chr2: 74,825,882-75,225,301 HK2, LINC01291, 10 more genes
    nsv6692636copy number variation1nstd229human GRCh38 chr2: 74,632,966-74,678,963 , GRCh37.p13 chr2: 74,860,093-74,906,090 M1AP, SEMA4F
    nsv6689149copy number variation1nstd229human GRCh38 chr2: 74,576,501-74,843,500 , GRCh37.p13 chr2: 74,803,628-75,070,627 LOC102724497, RPS28P5, 6 more genes
    nsv6688508copy number variation1nstd229human GRCh38 chr2: 74,592,565-74,749,791 , GRCh37.p13 chr2: 74,819,692-74,976,918 LOC102724497, TVP23BP2, 4 more genes
    nsv6687743copy number variation1nstd229human GRCh38 chr2: 74,556,901-74,565,900 , GRCh37.p13 chr2: 74,784,028-74,793,027 DOK1, M1AP
    nsv6687471copy number variation1nstd229human GRCh38 chr2: 74,619,387-74,626,038 , GRCh37.p13 chr2: 74,846,514-74,853,165 TOR1BP1, M1AP
    nsv6686690copy number variation1nstd229human GRCh38 chr2: 74,366,401-74,559,400 , GRCh37.p13 chr2: 74,593,528-74,786,527 DCTN1, CCDC142, 21 more genes
    nsv6684161copy number variation1nstd229human GRCh38 chr2: 74,623,329-74,639,495 , GRCh37.p13 chr2: 74,850,456-74,866,622 TVP23BP2, M1AP
    nsv6683749copy number variation1nstd229human GRCh38 chr2: 74,590,279-74,636,341 , GRCh37.p13 chr2: 74,817,406-74,863,468 M1AP, TOR1BP1, 1 more genes
    nsv6682530copy number variation1nstd229human GRCh38 chr2: 74,601,353-74,607,175 , GRCh37.p13 chr2: 74,828,480-74,834,302 M1AP
    nsv6682117copy number variation1nstd229human GRCh38 chr2: 74,590,524-74,594,100 , GRCh37.p13 chr2: 74,817,651-74,821,227 M1AP
    nsv6682095copy number variation1nstd229human GRCh38 chr2: 74,587,313-74,590,370 , GRCh37.p13 chr2: 74,814,440-74,817,497 M1AP
    nsv6681849copy number variation1nstd229human GRCh38 chr2: 74,593,093-75,089,574 , GRCh37.p13 chr2: 74,820,220-75,316,701 HK2, MIR5000, 12 more genes
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