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Items: 1 to 20 of 238

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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
    nsv5632279insertion1nstd207human GRCh38 chr10: 49,186,068-49,186,068 , GRCh37.p13 chr10: 50,394,113-50,394,113 TMEM273
    nsv5560635sequence alteration1nstd206human GRCh38 chr10: 49,163,978-49,173,434 , GRCh37.p13 chr10: 50,372,023-50,381,479 TMEM273
    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
    nsv5482918copy number variation1nstd206human GRCh38 chr10: 48,676,996-49,241,090 , GRCh37.p13 chr10: 49,885,041-50,449,135 FAM170B-AS1, LRRC18, 8 more genes
    nsv5479668copy number variation1nstd206human GRCh38 chr10: 49,157,585-49,171,501 , GRCh37.p13 chr10: 50,365,630-50,379,546 TMEM273
    nsv5478930copy number variation1nstd206human GRCh38 chr10: 49,163,948-49,168,758 , GRCh37.p13 chr10: 50,371,993-50,376,803 TMEM273
    nsv5478716copy number variation1nstd206human GRCh38 chr10: 49,167,708-49,168,336 , GRCh37.p13 chr10: 50,375,753-50,376,381 TMEM273
    nsv5475853copy number variation1nstd206human GRCh38 chr10: 49,159,575-49,159,996 , GRCh37.p13 chr10: 50,367,620-50,368,041 TMEM273
    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
    nsv5364913translocation1nstd200human GRCh38 chr10: 49,162,050-49,162,050 , GRCh38 chr10: 49,162,497-49,162,497 , GRCh37.p13 chr10: 50,370,095-50,370,095 , GRCh37.p13 chr10: 50,370,542-50,370,542 TMEM273
    nsv5337340translocation1nstd200human GRCh37 chr10: 50,370,542-50,370,542 , GRCh37 chr10: 50,370,095-50,370,095 , GRCh38.p12 chr10: 49,162,497-49,162,497 , GRCh38.p12 chr10: 49,162,050-49,162,050 TMEM273
    nsv5303787copy number variation1nstd204human GRCh38.p13 chr10: 49,167,745-49,168,345 , GRCh37.p13 chr10: 50,375,790-50,376,390 TMEM273
    nsv5256779copy number variation1nstd204human GRCh38.p13 chr10: 49,164,323-49,165,346 , GRCh37.p13 chr10: 50,372,368-50,373,391 TMEM273
    nsv5251575copy number variation1nstd204human GRCh38.p13 chr10: 49,182,229-49,210,844 , GRCh37.p13 chr10: 50,390,274-50,418,889 TMEM273
    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
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