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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5712968mobile element insertion1nstd211human GRCh38 chr10: 49,753,119-49,753,119 , GRCh37.p13 chr10: 50,961,165-50,961,165 OGDHL
    nsv5627766insertion1nstd207human GRCh38 chr10: 49,742,423-49,742,423 , GRCh37.p13 chr10: 50,950,469-50,950,469 OGDHL
    nsv5487262copy number variation1nstd206human GRCh38 chr10: 49,754,653-49,761,689 , GRCh37.p13 chr10: 50,962,699-50,969,735 OGDHL
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5380941copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,033,586-52,417,694 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 more genes
    nsv5241709copy number variation1nstd204human GRCh38.p13 chr10: 49,731,375-49,764,488 , GRCh37.p13 chr10: 50,939,421-50,972,534 OGDHL
    nsv5125554mobile element insertion1nstd203human GRCh38 chr10: 49,753,106-49,753,119 , GRCh37.p13 chr10: 50,961,152-50,961,165 OGDHL
    nsv5060032copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 46,966,535-51,874,356 , GRCh38.p12 chr10: 45,931,517-50,114,596 CHAT, CTSLP2, 104 more genes
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4969912copy number variation1nstd200human GRCh38 chr10: 49,753,209-49,753,776 , GRCh37.p13 chr10: 50,961,255-50,961,822 OGDHL
    nsv4969911copy number variation1nstd200human GRCh38 chr10: 49,745,181-49,747,187 , GRCh37.p13 chr10: 50,953,227-50,955,233 OGDHL
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4843946copy number variation1nstd200human GRCh37 chr10: 50,953,227-50,955,233 , GRCh38.p12 chr10: 49,745,181-49,747,187 OGDHL
    nsv4769372copy number variation1nstd102humanUncertain significance GRCh37 chr10: 49,391,938-51,053,159 , GRCh38.p12 chr10: 48,183,895-49,845,113 HSPD1P17, FAM170B-AS1, 27 more genes
    nsv4766133insertion1nstd199human GRCh37 chr10: 50,950,246-50,950,246 , GRCh38.p12 chr10: 49,742,200-49,742,200 OGDHL
    nsv4736384copy number variation1nstd199human GRCh37 chr10: 47,654,517-51,488,026 , GRCh38.p12 chr10: 45,931,517-49,929,364 , ARHGAP22-IT1, 99 more genes
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