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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147626insertion1nstd232human GRCh37.p13 chr14: 35,483,113-35,483,113 , GRCh38.p12 chr14: 35,013,907-35,013,907 SRP54
    nsv7143039insertion1nstd232human GRCh37.p13 chr14: 35,488,282-35,488,282 , GRCh38.p12 chr14: 35,019,076-35,019,076 SRP54
    nsv7143003insertion1nstd232human GRCh37.p13 chr14: 35,476,596-35,476,596 , GRCh38.p12 chr14: 35,007,390-35,007,390 SRP54
    nsv7137888insertion1nstd232human GRCh37.p13 chr14: 35,480,866-35,480,866 , GRCh38.p12 chr14: 35,011,660-35,011,660 SRP54
    nsv7094497copy number variation2nstd102humanUncertain significance GRCh37 chr14: 35,182,071-35,873,850 , GRCh38.p12 chr14: 34,712,865-35,404,644 NFKBIA, IGBP1P1, 19 more genes
    nsv7093467insertion1nstd102humanUncertain significance GRCh38 chr14: 35,011,659-35,011,659 , GRCh37 chr14: 35,480,865-35,480,865 SRP54
    nsv7093397copy number variation1nstd102humanPathogenic GRCh37 chr14: 34,904,407-36,784,136 , GRCh38.p12 chr14: 34,435,201-36,314,930 DPRXP3, LOC107984628, 51 more genes
    nsv7072225inversion1nstd229human GRCh38 chr14: 31,291,623-36,485,208 , GRCh37.p13 chr14: 31,760,829-36,954,413 LOC101927178, RNU7-93P, 84 more genes
    nsv7068575inversion1nstd229human GRCh38 chr14: 34,940,464-35,091,648 , GRCh37.p13 chr14: 35,409,670-35,560,854 PPP2R3C, IGBP1P1, 4 more genes
    nsv6957562copy number variation1nstd229human GRCh38 chr14: 34,796,766-35,163,366 , GRCh37.p13 chr14: 35,265,972-35,632,572 PRORP, FAM177A1, 10 more genes
    nsv6955674copy number variation1nstd229human GRCh38 chr14: 34,311,401-35,159,200 , GRCh37.p13 chr14: 34,780,607-35,628,406 SRP54, SPTSSA, 26 more genes
    nsv6955641copy number variation1nstd229human GRCh38 chr14: 34,924,660-35,315,430 , GRCh37.p13 chr14: 35,393,866-35,784,636 PRORP, IGBP1P1, 12 more genes
    nsv6948282copy number variation1nstd229human GRCh38 chr14: 34,998,801-35,068,200 , GRCh37.p13 chr14: 35,468,007-35,537,406 FAM177A1, SRP54
    nsv6946034copy number variation1nstd229human GRCh38 chr14: 34,979,076-35,080,666 , GRCh37.p13 chr14: 35,448,282-35,549,872 SRP54, SRP54-AS1, 2 more genes
    nsv6942660copy number variation1nstd229human GRCh38 chr14: 34,912,831-35,077,151 , GRCh37.p13 chr14: 35,382,037-35,546,357 SRP54, SRP54-AS1, 2 more genes
    nsv6939728copy number variation1nstd229human GRCh38 chr14: 34,836,903-35,282,666 , GRCh37.p13 chr14: 35,306,109-35,751,872 SEPTIN7P1, SRP54-AS1, 15 more genes
    nsv6591691inversion1nstd223human GRCh38 chr14: 35,026,917-35,027,090 , GRCh37.p13 chr14: 35,496,123-35,496,296 SRP54
    nsv6591442inversion1nstd223human GRCh38 chr14: 35,026,727-35,027,319 , GRCh37.p13 chr14: 35,495,933-35,496,525 SRP54
    nsv6589034inversion1nstd223human GRCh38 chr14: 35,021,413-35,022,591 , GRCh37.p13 chr14: 35,490,619-35,491,797 SRP54
    nsv6588469inversion1nstd223human GRCh38 chr14: 35,011,829-35,013,252 , GRCh37.p13 chr14: 35,481,035-35,482,458 SRP54
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