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Items: 1 to 20 of 164

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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
    nsv6992522copy number variation1nstd229human GRCh38 chr16: 56,624,546-56,624,592 , GRCh37.p13 chr16: 56,658,458-56,658,504 MT1E
    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
    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
    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
    nsv6512340copy number variation1nstd223human GRCh38 chr16: 56,627,001-56,633,900 , GRCh37.p13 chr16: 56,660,913-56,667,812 MT1JP, MT1M, 1 more genes
    nsv6507806copy number variation1nstd223human GRCh38 chr16: 56,626,578-56,633,514 , GRCh37.p13 chr16: 56,660,490-56,667,426 MT1E, MT1M
    nsv6507253copy number variation1nstd223human GRCh38 chr16: 56,618,054-56,626,343 , GRCh37.p13 chr16: 56,651,966-56,660,255 MT1L, MT1E
    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
    nsv6504814copy number variation1nstd223human GRCh38 chr16: 56,621,050-56,630,256 , GRCh37.p13 chr16: 56,654,962-56,664,168 MT1E
    nsv6497437copy number variation1nstd223human GRCh38 chr16: 56,626,953-56,633,824 , GRCh37.p13 chr16: 56,660,865-56,667,736 MT1M, MT1E, 1 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
    nsv6250313mobile element insertion1nstd215human GRCh38 chr16: 56,627,048-56,627,048 , GRCh37.p13 chr16: 56,660,960-56,660,960 MT1E
    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
    nsv6088649insertion1nstd212human GRCh38 chr16: 56,627,032-56,627,032 , GRCh37.p13 chr16: 56,660,944-56,660,944 MT1E
    nsv5976967insertion1nstd209human GRCh38 chr16: 56,624,558-56,624,558 , GRCh37.p13 chr16: 56,658,470-56,658,470 MT1E
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