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Items: 1 to 20 of 464

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968604inversion1nstd209human GRCh38 chr2: 49,436,021-59,087,697 , GRCh37.p13 chr2: 49,663,159-59,314,832 , ACYP2, 95 more genes
    nsv5883814copy number variation1nstd209human GRCh38 chr2: 55,096,718-55,109,685 , GRCh37.p13 chr2: 55,323,854-55,336,821 RTN4
    nsv5882713copy number variation1nstd209human GRCh38 chr2: 55,015,538-55,015,674 , GRCh37.p13 chr2: 55,242,674-55,242,810 RTN4
    nsv5833401copy number variation1nstd209human GRCh38 chr2: 55,096,687-55,109,719 , GRCh37.p13 chr2: 55,323,823-55,336,855 RTN4
    nsv5725826mobile element insertion2nstd211human GRCh38 chr2: 55,065,393-55,065,393 , GRCh37.p13 chr2: 55,292,529-55,292,529 RTN4
    nsv5714329mobile element insertion2nstd211human GRCh38 chr2: 55,041,000-55,041,000 , GRCh37.p13 chr2: 55,268,136-55,268,136 RTN4
    nsv5692242mobile element insertion1nstd211human GRCh38 chr2: 55,017,169-55,017,169 , GRCh37.p13 chr2: 55,244,305-55,244,305 RTN4
    nsv5690021mobile element insertion1nstd211human GRCh38 chr2: 55,073,154-55,073,154 , GRCh37.p13 chr2: 55,300,290-55,300,290 RTN4
    nsv5608608insertion1nstd207human GRCh38 chr2: 55,061,066-55,061,066 , GRCh37.p13 chr2: 55,288,202-55,288,202 RTN4
    nsv5561532inversion1nstd206human GRCh38 chr2: 55,066,622-55,069,188 , GRCh37.p13 chr2: 55,293,758-55,296,324 RTN4
    nsv5559913sequence alteration1nstd206human GRCh38 chr2: 55,044,536-55,044,537 , GRCh37.p13 chr2: 55,271,672-55,271,673 RTN4
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5544408insertion1nstd206human GRCh38 chr2: 55,044,536-55,044,536 , GRCh37.p13 chr2: 55,271,672-55,271,672 RTN4
    nsv5448358copy number variation1nstd206human GRCh38 chr2: 55,096,719-55,109,686 , GRCh37.p13 chr2: 55,323,855-55,336,822 RTN4
    nsv5440091copy number variation1nstd206human GRCh38 chr2: 55,118,201-55,125,825 , GRCh37.p13 chr2: 55,345,337-55,352,961 RTN4
    nsv5410370mobile element insertion1nstd206human GRCh38 chr2: 55,073,154-55,073,205 , GRCh37.p13 chr2: 55,300,290-55,300,341 RTN4
    nsv5366221translocation1nstd200human GRCh37.p13 chr2: 55,362,187-55,362,187 , GRCh38 chr2: 55,135,051-55,135,051 , GRCh38 chr20: 25,249,287-25,249,287 , GRCh37.p13 chr20: 25,229,923-25,229,923 PYGB, RTN4
    nsv5366218translocation1nstd200human GRCh38 chr2: 55,134,732-55,134,732 , GRCh38 chr20: 25,249,285-25,249,285 , GRCh37.p13 chr2: 55,361,868-55,361,868 , GRCh37.p13 chr20: 25,229,921-25,229,921 PYGB, RTN4
    nsv5344207translocation1nstd200human GRCh37 chr2: 55,205,604-55,205,604 , GRCh37 chr2: 55,205,552-55,205,552 , GRCh38.p12 chr2: 54,978,416-54,978,416 , GRCh38.p12 chr2: 54,978,468-54,978,468 RTN4
    nsv5212745copy number variation1nstd204human GRCh38.p13 chr2: 55,075,785-55,078,384 , GRCh37.p13 chr2: 55,302,921-55,305,520 RTN4, LOC105374662
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