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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074176inversion1nstd229human GRCh38 chr14: 51,929,058-52,008,558 , GRCh37.p13 chr14: 52,395,776-52,475,276 NID2, RTRAF, 2 more genes
    nsv7074157inversion1nstd229human GRCh38 chr14: 51,800,664-53,760,846 , GRCh37.p13 chr14: 52,267,382-54,227,564 GNPNAT1, LOC102723604, 26 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7060630inversion1nstd229human GRCh38 chr14: 52,064,707-52,703,250 , GRCh37.p13 chr14: 52,531,425-53,169,968 LOC105378180, GPR137C, 8 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6955943copy number variation1nstd229human GRCh38 chr14: 52,040,140-52,047,954 , GRCh37.p13 chr14: 52,506,858-52,514,672 NID2
    nsv6952850copy number variation1nstd229human GRCh38 chr14: 52,009,201-52,020,100 , GRCh37.p13 chr14: 52,475,919-52,486,818 NID2, RTRAF
    nsv6952607copy number variation1nstd229human GRCh38 chr14: 52,002,292-52,037,827 , GRCh37.p13 chr14: 52,469,010-52,504,545 RTRAF, NID2
    nsv6952329copy number variation1nstd229human GRCh38 chr14: 52,041,416-52,044,956 , GRCh37.p13 chr14: 52,508,134-52,511,674 NID2
    nsv6949862copy number variation1nstd229human GRCh38 chr14: 51,123,112-56,995,885 , GRCh37.p13 chr14: 51,589,830-57,462,603 RPL3P3, RNA5SP385, 96 more genes
    nsv6947643copy number variation1nstd229human GRCh38 chr14: 51,488,373-52,092,682 , GRCh37.p13 chr14: 51,955,091-52,559,400 NID2, LOC102723604, 14 more genes
    nsv6945481copy number variation1nstd229human GRCh38 chr14: 52,012,850-52,035,533 , GRCh37.p13 chr14: 52,479,568-52,502,251 NID2
    nsv6945259copy number variation1nstd229human GRCh38 chr14: 52,004,655-52,166,397 , GRCh37.p13 chr14: 52,471,373-52,633,115 RTRAF, NID2, 3 more genes
    nsv6942276copy number variation1nstd229human GRCh38 chr14: 52,046,093-52,065,059 , GRCh37.p13 chr14: 52,512,811-52,531,777 NID2
    nsv6941022copy number variation1nstd229human GRCh38 chr14: 52,004,982-52,005,264 , GRCh37.p13 chr14: 52,471,700-52,471,982 NID2, RTRAF
    nsv6938412copy number variation1nstd229human GRCh38 chr14: 46,367,427-52,468,480 , GRCh37.p13 chr14: 46,836,630-52,935,198 RNU6-297P, RN7SL452P, 95 more genes
    nsv6578746inversion1nstd223human GRCh38 chr14: 49,838,941-56,572,992 , GRCh37.p13 chr14: 50,305,659-57,039,710 LOC100419913, TXNDC16, 124 more genes
    nsv6489336copy number variation1nstd223human GRCh38 chr14: 52,040,140-52,047,949 , GRCh37.p13 chr14: 52,506,858-52,514,667 NID2
    nsv6478288copy number variation1nstd223human GRCh38 chr14: 52,046,093-52,065,058 , GRCh37.p13 chr14: 52,512,811-52,531,776 NID2
    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
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