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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7063904inversion1nstd229human GRCh38 chr16: 54,352,554-57,044,545 , GRCh37.p13 chr16: 54,386,466-57,078,457 LOC102725116, OGFOD1, 65 more genes
    nsv6992844copy number variation1nstd229human GRCh38 chr16: 56,637,408-56,643,696 , GRCh37.p13 chr16: 56,671,320-56,677,608 MT1DP, MT1A, 1 more genes
    nsv6988213copy number variation1nstd229human GRCh38 chr16: 56,626,479-56,683,243 , GRCh37.p13 chr16: 56,660,391-56,717,155 LOC101927536, MT1X, 11 more genes
    nsv6981044copy number variation1nstd229human GRCh38 chr16: 56,635,912-56,644,208 , GRCh37.p13 chr16: 56,669,824-56,678,120 MT1DP, MT1A, 1 more genes
    nsv6980863copy number variation1nstd229human GRCh38 chr16: 56,619,201-56,661,100 , GRCh37.p13 chr16: 56,653,113-56,695,012 MT1F, MT1CP, 8 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6623866copy number variation1nstd224human GRCh37 chr16: 56,673,143-56,716,982 , GRCh38.p12 chr16: 56,639,231-56,683,070 MT1A, MT1H, 8 more genes
    nsv6623722copy number variation1nstd224human GRCh37 chr16: 56,659,783-56,697,798 , GRCh38.p12 chr16: 56,625,871-56,663,886 MT1A, MT1B, 7 more genes
    nsv6623680copy number variation3nstd224human GRCh37 chr16: 56,667,294-56,716,982 , GRCh38.p12 chr16: 56,633,382-56,683,070 MT1B, MT1H, 10 more genes
    nsv6507204copy number variation1nstd223human GRCh38 chr16: 56,626,482-56,683,243 , GRCh37.p13 chr16: 56,660,394-56,717,155 MT1CP, MT1A, 11 more genes
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5929985copy number variation1nstd209human GRCh38 chr16: 56,619,255-56,661,122 , GRCh37.p13 chr16: 56,653,167-56,695,034 MT1DP, MT1A, 8 more genes
    nsv5886009copy number variation2nstd209human GRCh38 chr16: 56,645,337-56,647,436 , GRCh37.p13 chr16: 56,679,249-56,681,348 MT1CP, MT1DP
    nsv5885009copy number variation1nstd209human GRCh38 chr16: 56,619,240-56,660,960 , GRCh37.p13 chr16: 56,653,152-56,694,872 LOC101927536, MT1E, 8 more genes
    nsv5525141copy number variation1nstd206human GRCh38 chr16: 56,626,482-56,683,244 , GRCh37.p13 chr16: 56,660,394-56,717,156 MT1B, MT1H, 11 more genes
    nsv5314506copy number variation1nstd204human GRCh38.p13 chr16: 56,626,187-56,683,500 , GRCh37.p13 chr16: 56,660,099-56,717,412 MT1F, MT1CP, 11 more genes
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