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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6975681copy number variation1nstd229human GRCh38 chr14: 70,562,447-70,774,880 , GRCh37.p13 chr14: 71,029,164-71,241,597 ADAM20, RN7SL77P, 7 more genes
    nsv6966951copy number variation1nstd229human GRCh38 chr14: 70,353,016-71,619,916 , GRCh37.p13 chr14: 70,819,733-72,086,633 LOC100420563, LOC105370556, 30 more genes
    nsv6962409copy number variation1nstd229human GRCh38 chr14: 70,655,252-70,657,825 , GRCh37.p13 chr14: 71,121,969-71,124,542 TTC9
    nsv6962027copy number variation1nstd229human GRCh38 chr14: 70,649,848-70,654,791 , GRCh37.p13 chr14: 71,116,565-71,121,508 TTC9
    nsv6960198copy number variation1nstd229human GRCh38 chr14: 70,487,310-70,752,569 , GRCh37.p13 chr14: 70,954,027-71,219,286 MED6, RNU6-659P, 10 more genes
    nsv6595203inversion1nstd223human GRCh38 chr14: 70,475,726-71,848,465 , GRCh37.p13 chr14: 70,942,443-72,315,182 TTC9-DT, MED6, 25 more genes
    nsv6578155inversion1nstd223human GRCh38 chr14: 70,650,425-70,651,152 , GRCh37.p13 chr14: 71,117,142-71,117,869 TTC9
    nsv6492096copy number variation1nstd223human GRCh38 chr14: 70,641,501-70,643,800 , GRCh37.p13 chr14: 71,108,218-71,110,517 TTC9, TTC9-DT
    nsv6481464copy number variation1nstd223human GRCh38 chr14: 70,654,450-70,655,251 , GRCh37.p13 chr14: 71,121,167-71,121,968 TTC9
    nsv6480485copy number variation1nstd223human GRCh38 chr14: 70,640,601-70,643,100 , GRCh37.p13 chr14: 71,107,318-71,109,817 TTC9-DT, TTC9
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 more genes
    nsv6475778copy number variation1nstd223human GRCh38 chr14: 70,655,201-70,657,900 , GRCh37.p13 chr14: 71,121,918-71,124,617 TTC9
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6241497mobile element insertion1nstd215human GRCh38 chr14: 70,643,060-70,643,060 , GRCh37.p13 chr14: 71,109,777-71,109,777 TTC9
    nsv6132791copy number variation1nstd213human GRCh37 chr14: 70,880,000-72,150,001 , GRCh38.p12 chr14: 70,413,283-71,683,284 MED6, SYNJ2BP, 28 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5509643copy number variation1nstd206human GRCh38 chr14: 70,654,360-70,655,231 , GRCh37.p13 chr14: 71,121,077-71,121,948 TTC9
    nsv5506017copy number variation1nstd206human GRCh38 chr14: 70,642,075-70,642,126 , GRCh37.p13 chr14: 71,108,792-71,108,843 TTC9
    nsv5496517copy number variation1nstd206human GRCh38 chr14: 70,655,252-70,657,761 , GRCh37.p13 chr14: 71,121,969-71,124,478 TTC9
    nsv5374597translocation1nstd200human GRCh38 chr14: 70,657,768-70,657,768 , GRCh38 chr14: 70,655,253-70,655,253 , GRCh37.p13 chr14: 71,124,485-71,124,485 , GRCh37.p13 chr14: 71,121,970-71,121,970 TTC9
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