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Items: 1 to 20 of 558

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131352insertion1nstd186human GRCh37 chr17: 43,991,589-43,991,622 , GRCh38.p12 chr17|NT_187663.1: 616,338-616,371 , GRCh38.p12 chr17: 45,914,223-45,914,256 MAPT
    nsv5976645insertion1nstd209human GRCh38 chr17: 45,914,205-45,914,205 , GRCh37.p13 chr17: 43,991,571-43,991,571 MAPT
    nsv5971659inversion1nstd209human GRCh38 chr17: 45,709,543-46,285,600 , GRCh37.p13 chr17: 43,786,909-44,362,966 CRHR1, MAPT, 14 more genes
    nsv5943855copy number variation1nstd209human GRCh38 chr17: 45,927,053-45,927,172 , GRCh37.p13 chr17: 44,004,419-44,004,538 LOC105371800, MAPT
    nsv5937206copy number variation1nstd209human GRCh38 chr17: 45,613,816-46,277,009 , GRCh37.p13 chr17: 43,691,182-44,354,375 LOC100132570, MAPT-IT1, 17 more genes
    nsv5672416inversion1nstd207human GRCh37.p13 chr17: 43,642,735-44,574,574 , GRCh38 chr17: 45,565,369-46,497,208 , CRHR1, 25 more genes
    nsv5669290inversion1nstd207human GRCh37.p13 chr17: 43,651,055-44,369,411 , GRCh38 chr17: 45,573,689-46,292,045 CRHR1, MAPT, 21 more genes
    nsv5663809insertion1nstd207human GRCh38 chr17: 45,941,717-45,941,717 , GRCh37.p13 chr17: 44,019,083-44,019,083 MAPT
    nsv5663362insertion1nstd207human GRCh38 chr17: 45,904,135-45,904,135 , GRCh37.p13 chr17: 43,981,501-43,981,501 MAPT
    nsv5661178insertion1nstd207human GRCh38 chr17: 45,914,205-45,914,205 , GRCh37.p13 chr17: 43,991,571-43,991,571 MAPT
    nsv5658786insertion1nstd207human GRCh38 chr17: 45,903,878-45,903,878 , GRCh37.p13 chr17: 43,981,244-43,981,244 MAPT
    nsv5645627insertion1nstd207human GRCh38 chr17: 45,941,685-45,941,685 , GRCh37.p13 chr17: 44,019,051-44,019,051 MAPT
    nsv5603570copy number variation1nstd207human GRCh38 chr17: 45,903,755-45,903,831 , GRCh37.p13 chr17: 43,981,121-43,981,197 MAPT
    nsv5602604copy number variation1nstd207human GRCh38 chr17: 45,904,035-45,904,097 , GRCh37.p13 chr17: 43,981,401-43,981,463 MAPT
    nsv5599644copy number variation1nstd207human GRCh38 chr17: 46,009,357-46,009,594 , GRCh37.p13 chr17: 44,086,723-44,086,960 MAPT
    nsv5598124copy number variation1nstd207human GRCh38 chr17: 45,969,502-45,969,604 , GRCh37.p13 chr17: 44,046,868-44,046,970 MAPT
    nsv5596574copy number variation1nstd207human GRCh38 chr17: 45,904,260-45,904,337 , GRCh37.p13 chr17: 43,981,626-43,981,703 MAPT
    nsv5559068sequence alteration1nstd206human GRCh38 chr17: 45,585,847-46,260,627 , GRCh37.p13 chr17: 43,663,213-44,337,993 KANSL1, MAPK8IP1P1, 19 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5545014insertion1nstd206human GRCh38 chr17: 45,914,223-45,914,256 , GRCh37.p13 chr17: 43,991,589-43,991,622 MAPT
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