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Items: 1 to 20 of 809

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142528copy number variation1nstd232human GRCh37.p13 chr7: 38,580,887-38,580,937 , GRCh38.p12 chr7: 38,541,287-38,541,337 AMPH
    nsv7049695inversion1nstd229human GRCh38 chr7: 38,385,394-38,387,078 , GRCh37.p13 chr7: 38,424,995-38,426,679 AMPH
    nsv7042482inversion1nstd229human GRCh38 chr7: 38,373,006-38,383,013 , GRCh37.p13 chr7: 38,412,607-38,422,614 AMPH, TRG-AS1
    nsv6836325copy number variation1nstd229human GRCh38 chr7: 38,514,737-38,518,321 , GRCh37.p13 chr7: 38,554,337-38,557,921 AMPH
    nsv6836272copy number variation1nstd229human GRCh38 chr7: 38,598,912-38,604,656 , GRCh37.p13 chr7: 38,638,512-38,644,256 AMPH
    nsv6835268copy number variation1nstd229human GRCh38 chr7: 38,402,984-38,407,232 , GRCh37.p13 chr7: 38,442,584-38,446,832 AMPH
    nsv6834665copy number variation1nstd229human GRCh38 chr7: 38,582,639-38,612,982 , GRCh37.p13 chr7: 38,622,239-38,652,582 AMPH
    nsv6833342copy number variation1nstd229human GRCh38 chr7: 38,509,596-38,519,330 , GRCh37.p13 chr7: 38,549,196-38,558,930 AMPH
    nsv6832204copy number variation1nstd229human GRCh38 chr7: 38,614,355-38,616,311 , GRCh37.p13 chr7: 38,653,955-38,655,911 AMPH
    nsv6831396copy number variation1nstd229human GRCh38 chr7: 38,580,824-38,581,205 , GRCh37.p13 chr7: 38,620,424-38,620,805 AMPH
    nsv6831029copy number variation1nstd229human GRCh38 chr7: 38,621,701-38,719,300 , GRCh37.p13 chr7: 38,661,301-38,758,900 KRT8P20, CFAP144P1, 1 more genes
    nsv6829566copy number variation1nstd229human GRCh38 chr7: 38,459,225-38,460,626 , GRCh37.p13 chr7: 38,498,825-38,500,226 AMPH
    nsv6829543copy number variation1nstd229human GRCh38 chr7: 38,512,123-38,521,939 , GRCh37.p13 chr7: 38,551,723-38,561,539 AMPH
    nsv6828496copy number variation1nstd229human GRCh38 chr7: 38,541,289-38,541,338 , GRCh37.p13 chr7: 38,580,889-38,580,938 AMPH
    nsv6828259copy number variation1nstd229human GRCh38 chr7: 38,520,081-38,525,921 , GRCh37.p13 chr7: 38,559,681-38,565,521 AMPH
    nsv6827892copy number variation1nstd229human GRCh38 chr7: 38,454,617-38,456,162 , GRCh37.p13 chr7: 38,494,217-38,495,762 AMPH
    nsv6827319copy number variation1nstd229human GRCh38 chr7: 38,517,808-38,518,074 , GRCh37.p13 chr7: 38,557,408-38,557,674 AMPH
    nsv6826261copy number variation1nstd229human GRCh38 chr7: 38,494,881-38,785,949 , GRCh37.p13 chr7: 38,534,481-38,825,549 RN7SL83P, KRT8P20, 3 more genes
    nsv6826152copy number variation1nstd229human GRCh38 chr7: 38,451,292-38,451,355 , GRCh37.p13 chr7: 38,490,892-38,490,955 AMPH
    nsv6825597copy number variation1nstd229human GRCh38 chr7: 38,626,869-38,627,262 , GRCh37.p13 chr7: 38,666,469-38,666,862 AMPH
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