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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7143760insertion1nstd232human GRCh37.p13 chr6: 123,924,306-123,924,306 , GRCh38.p12 chr6: 123,603,161-123,603,161 TRDN
    nsv7137202copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,713,854-124,105,184 , GRCh38.p12 chr6: 112,392,652-123,784,039 COL10A1, FABP7, 129 more genes
    nsv7097571copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,851,631-123,868,537 , GRCh38.p12 chr6: 123,530,486-123,547,392 LOC105377982, TRDN
    nsv7097570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,637,582-123,673,751 , GRCh38.p12 chr6: 123,316,437-123,352,606 TRDN, LOC105377984
    nsv7097569copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,580,749-123,595,835 , GRCh38.p12 chr6: 123,259,604-123,274,690 TRDN
    nsv7097568copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,573,537-123,573,600 , GRCh38.p12 chr6: 123,252,392-123,252,455 TRDN
    nsv7097567copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,539,746-123,833,527 , GRCh38.p12 chr6: 123,218,601-123,512,382 TRDN, TRDN-AS1, 1 more genes
    nsv7097314copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,851,631-123,851,730 , GRCh38.p12 chr6: 123,530,486-123,530,585 TRDN, LOC105377982
    nsv7097313copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,703,243-123,703,312 , GRCh38.p12 chr6: 123,382,098-123,382,167 TRDN
    nsv7097312copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,687,260-123,687,347 , GRCh38.p12 chr6: 123,366,115-123,366,202 TRDN
    nsv7097178copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,818,318-123,825,066 , GRCh38.p12 chr6: 123,497,173-123,503,921 TRDN
    nsv7097177copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,581,737-123,581,803 , GRCh38.p12 chr6: 123,260,592-123,260,658 TRDN
    nsv7097037copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,833,428-123,837,371 , GRCh38.p12 chr6: 123,512,283-123,516,226 TRDN
    nsv7093381copy number variation1nstd102humannot provided GRCh37 chr6: 119,243,634-126,078,530 , GRCh38.p12 chr6: 118,922,469-125,757,384 HEY2-AS1, SERINC1, 52 more genes
    nsv7057513inversion1nstd229human GRCh38 chr6: 123,412,065-123,412,153 , GRCh37.p13 chr6: 123,733,210-123,733,298 TRDN
    nsv7055222inversion1nstd229human GRCh38 chr6: 123,290,013-123,292,571 , GRCh37.p13 chr6: 123,611,158-123,613,716 TRDN
    nsv7051442inversion1nstd229human GRCh38 chr6: 120,525,437-125,245,762 , GRCh37.p13 chr6: 120,846,583-125,566,908 RNF217-AS1, HSF2, 35 more genes
    nsv7050325inversion1nstd229human GRCh38 chr6: 123,443,338-123,446,434 , GRCh37.p13 chr6: 123,764,483-123,767,579 TRDN, TRDN-AS1
    nsv7048680inversion1nstd229human GRCh38 chr6: 120,128,256-123,693,128 , GRCh37.p13 chr6: 120,449,402-124,014,273 TRDN-AS1, TBC1D32, 30 more genes
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