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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950065insertion1nstd209human GRCh38 chr2: 197,675,604-197,675,604 , GRCh37.p13 chr2: 198,540,328-198,540,328 RFTN2
    nsv5948052insertion1nstd209human GRCh38 chr2: 197,665,517-197,665,517 , GRCh37.p13 chr2: 198,530,241-198,530,241 RFTN2
    nsv5906114copy number variation1nstd209human GRCh38 chr2: 197,619,115-197,619,224 , GRCh37.p13 chr2: 198,483,839-198,483,948 RFTN2
    nsv5899783copy number variation1nstd209human GRCh38 chr2: 197,623,319-197,623,372 , GRCh37.p13 chr2: 198,488,043-198,488,096 RFTN2
    nsv5897294copy number variation1nstd209human GRCh38 chr2: 197,603,896-197,603,966 , GRCh37.p13 chr2: 198,468,620-198,468,690 RFTN2
    nsv5889435copy number variation1nstd209human GRCh38 chr2: 197,591,080-197,591,199 , GRCh37.p13 chr2: 198,455,804-198,455,923 RFTN2
    nsv5831841copy number variation1nstd209human GRCh38 chr2: 197,602,697-197,605,784 , GRCh37.p13 chr2: 198,467,421-198,470,508 RFTN2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5446059copy number variation1nstd206human GRCh38 chr2: 197,603,897-197,603,967 , GRCh37.p13 chr2: 198,468,621-198,468,691 RFTN2
    nsv5444752copy number variation1nstd206human GRCh38 chr2: 197,652,509-197,657,980 , GRCh37.p13 chr2: 198,517,233-198,522,704 RFTN2
    nsv5443107copy number variation1nstd206human GRCh38 chr2: 197,618,182-197,618,421 , GRCh37.p13 chr2: 198,482,906-198,483,145 RFTN2
    nsv5441226copy number variation1nstd206human GRCh38 chr2: 197,664,663-197,670,304 , GRCh37.p13 chr2: 198,529,387-198,535,028 RFTN2
    nsv5439026copy number variation1nstd206human GRCh38 chr2: 197,618,859-197,618,969 , GRCh37.p13 chr2: 198,483,583-198,483,693 RFTN2
    nsv5351167translocation1nstd200human GRCh38 chr2: 197,616,823-197,616,823 , GRCh38 chr2: 197,617,061-197,617,061 , GRCh37.p13 chr2: 198,481,785-198,481,785 , GRCh37.p13 chr2: 198,481,547-198,481,547 RFTN2
    nsv5310771copy number variation1nstd204human GRCh38.p13 chr2: 197,602,563-197,607,350 , GRCh37.p13 chr2: 198,467,287-198,472,074 RFTN2
    nsv5307422copy number variation1nstd204human GRCh38.p13 chr2: 197,583,886-197,585,476 , GRCh37.p13 chr2: 198,448,610-198,450,200 RFTN2
    nsv5218910copy number variation1nstd204human GRCh38.p13 chr2: 197,600,101-197,606,600 , GRCh37.p13 chr2: 198,464,825-198,471,324 RFTN2
    nsv5218769copy number variation1nstd204human GRCh38.p13 chr2: 197,602,147-197,608,478 , GRCh37.p13 chr2: 198,466,871-198,473,202 RFTN2
    nsv5214468copy number variation1nstd204human GRCh38.p13 chr2: 197,605,059-197,607,603 , GRCh37.p13 chr2: 198,469,783-198,472,327 RFTN2
    nsv5205769copy number variation1nstd204human GRCh38.p13 chr2: 197,588,997-197,591,096 , GRCh37.p13 chr2: 198,453,721-198,455,820 RFTN2
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