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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7057325inversion1nstd229human GRCh38 chr3: 170,134,629-173,143,661 , GRCh37.p13 chr3: 169,852,417-172,861,451 LINC02068, LOC107986052, 45 more genes
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv6734429copy number variation1nstd229human GRCh38 chr3: 171,857,830-171,858,741 , GRCh37.p13 chr3: 171,575,620-171,576,531 TMEM212
    nsv6725210copy number variation1nstd229human GRCh38 chr3: 171,842,472-171,846,297 , GRCh37.p13 chr3: 171,560,262-171,564,087 TMEM212
    nsv6724169copy number variation1nstd229human GRCh38 chr3: 171,827,563-171,910,946 , GRCh37.p13 chr3: 171,545,353-171,628,736 TMEM212, LOC105374218, 1 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636786copy number variation1nstd102humanUncertain significance GRCh37 chr3: 171,217,561-171,732,049 , GRCh38.p12 chr3: 171,499,772-172,014,259 TMEM212, LOC105374217, 4 more genes
    nsv6636579copy number variation1nstd102humanUncertain significance GRCh37 chr3: 171,264,604-171,567,019 , GRCh38.p12 chr3: 171,546,815-171,849,229 TMEM212, PLD1
    nsv6636335copy number variation1nstd102humanUncertain significance GRCh37 chr3: 171,340,993-171,685,216 , GRCh38.p12 chr3: 171,623,203-171,967,426 LOC105374217, TMEM212, 3 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6374539copy number variation1nstd223human GRCh38 chr3: 171,857,828-171,858,742 , GRCh37.p13 chr3: 171,575,618-171,576,532 TMEM212
    nsv6367961copy number variation1nstd223human GRCh38 chr3: 171,856,041-171,856,710 , GRCh37.p13 chr3: 171,573,831-171,574,500 TMEM212
    nsv6361920copy number variation1nstd223human GRCh38 chr3: 171,842,472-171,846,297 , GRCh37.p13 chr3: 171,560,262-171,564,087 TMEM212
    nsv6298455copy number variation1nstd186human GRCh37 chr3: 171,575,618-171,576,532 , GRCh38.p12 chr3: 171,857,828-171,858,742 TMEM212
    nsv6291110copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 168,118,411-179,867,071 , GRCh38.p12 chr3: 168,400,623-180,149,283 ACTL6A, ECT2, 141 more genes
    nsv6134792copy number variation1nstd213human GRCh37 chr3: 169,810,000-174,480,001 , GRCh38.p12 chr3: 170,092,212-174,762,211 ECT2, SKIL, 56 more genes
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5887721copy number variation1nstd209human GRCh38 chr3: 171,857,828-171,858,737 , GRCh37.p13 chr3: 171,575,618-171,576,527 TMEM212
    nsv5690869mobile element insertion1nstd211human GRCh38 chr3: 171,854,649-171,854,649 , GRCh37.p13 chr3: 171,572,439-171,572,439 TMEM212
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