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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7068595inversion1nstd229human GRCh38 chr10: 45,208,870-45,507,407 , GRCh37.p13 chr10: 45,704,318-46,002,855 ALOX5, OR6D1P, 6 more genes
    nsv7060234inversion1nstd229human GRCh38 chr10: 45,095,166-45,498,206 , GRCh37.p13 chr10: 45,590,614-45,993,654 ALOX5, ANKRD30BP3, 12 more genes
    nsv6895651copy number variation1nstd229human GRCh38 chr10: 44,205,517-45,550,271 , GRCh37.p13 chr10: 44,700,965-46,045,719 OR13A1, RPL9P21, 27 more genes
    nsv6891570copy number variation1nstd229human GRCh38 chr10: 45,406,863-45,457,337 , GRCh37.p13 chr10: 45,902,311-45,952,785 MARCHF8, LOC102724323, 1 more genes
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6882722copy number variation1nstd229human GRCh38 chr10: 45,286,474-45,554,400 , GRCh37.p13 chr10: 45,781,922-46,049,848 ALOX5, OR13A1, 3 more genes
    nsv6881291copy number variation1nstd229human GRCh38 chr10: 45,443,401-45,445,600 , GRCh37.p13 chr10: 45,938,849-45,941,048 LOC102724323, ALOX5
    nsv6450364copy number variation1nstd223human GRCh38 chr10: 45,450,031-45,452,856 , GRCh37.p13 chr10: 45,945,479-45,948,304 MARCHF8, LOC102724323
    nsv6449246copy number variation1nstd223human GRCh38 chr10: 45,417,564-45,580,990 , GRCh37.p13 chr10: 45,913,012-46,076,438 LOC102724323, ALOX5, 2 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv5925806copy number variation1nstd209human GRCh38 chr10: 45,443,503-45,443,675 , GRCh37.p13 chr10: 45,938,951-45,939,123 LOC102724323, ALOX5
    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
    nsv4973599copy number variation1nstd200human GRCh38 chr10: 45,417,564-45,580,990 , GRCh37.p13 chr10: 45,913,012-46,076,438 LOC102724323, MARCHF8, 2 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4769357copy number variation1nstd102humanUncertain significance GRCh37 chr10: 45,758,657-46,021,583 , GRCh38.p12 chr10|NW_003315935.1: 87,977-309,802 , GRCh38.p12 chr10: 45,263,209-45,526,135 ALOX5, OR13A1, 3 more genes
    nsv4479970mobile element insertion1nstd166human GRCh37.p13 chr10: 45,948,451-45,948,451 , GRCh38.p12 chr10: 45,453,003-45,453,003 , GRCh38.p12 chr10|NW_003315935.1: 293,834-293,834 MARCHF8, LOC102724323
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
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