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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097553copy number variation1nstd102humanPathogenic GRCh37 chr5: 94,800,311-96,107,383 , GRCh38.p12 chr5: 95,464,607-96,771,679 LOC105379675, GPR150, 27 more genes
    nsv7058036inversion1nstd229human GRCh38 chr5: 94,195,543-97,660,538 , GRCh37.p13 chr5: 93,531,248-96,996,242 RIOK2, SPATA9, 51 more genes
    nsv7054048inversion1nstd229human GRCh38 chr5: 95,786,828-95,790,048 , GRCh37.p13 chr5: 95,122,532-95,125,752 RHOBTB3
    nsv7045134inversion1nstd229human GRCh38 chr5: 95,722,347-95,722,397 , GRCh37.p13 chr5: 95,058,051-95,058,101 SPATA9, RHOBTB3
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv6773004copy number variation1nstd229human GRCh38 chr5: 94,767,305-97,708,544 , GRCh37.p13 chr5: 94,103,010-97,044,248 FABP5P5, SPATA9, 45 more genes
    nsv6770732copy number variation1nstd229human GRCh38 chr5: 95,768,680-95,951,039 , GRCh37.p13 chr5: 95,104,384-95,286,743 LOC105379091, GLRX, 6 more genes
    nsv6767910copy number variation1nstd229human GRCh38 chr5: 95,756,896-95,759,898 , GRCh37.p13 chr5: 95,092,600-95,095,602 RHOBTB3
    nsv6767196copy number variation1nstd229human GRCh38 chr5: 95,464,994-96,106,661 , GRCh37.p13 chr5: 94,800,698-95,442,365 ELL2, ARSK, 19 more genes
    nsv6763578copy number variation1nstd229human GRCh38 chr5: 95,771,001-95,785,900 , GRCh37.p13 chr5: 95,106,705-95,121,604 RHOBTB3, HSPD1P11
    nsv6763127copy number variation1nstd229human GRCh38 chr5: 95,710,508-95,715,092 , GRCh37.p13 chr5: 95,046,212-95,050,796 SPATA9, RHOBTB3
    nsv6762687copy number variation1nstd229human GRCh38 chr5: 95,756,589-95,798,698 , GRCh37.p13 chr5: 95,092,293-95,134,402 HSPD1P11, RHOBTB3
    nsv6758727copy number variation1nstd229human GRCh38 chr5: 95,767,444-95,775,322 , GRCh37.p13 chr5: 95,103,148-95,111,026 RHOBTB3, HSPD1P11
    nsv6630453copy number variation1nstd224human GRCh37 chr5: 95,072,623-95,423,944 , GRCh38.p12 chr5: 95,736,919-96,088,240 GLRX, LINC01554, 11 more genes
    nsv6565348inversion1nstd223human GRCh38 chr5: 95,782,508-95,783,195 , GRCh37.p13 chr5: 95,118,212-95,118,899 RHOBTB3
    nsv6562850inversion1nstd223human GRCh38 chr5: 95,782,704-95,783,361 , GRCh37.p13 chr5: 95,118,408-95,119,065 RHOBTB3
    nsv6410812copy number variation1nstd223human GRCh38 chr5: 95,381,684-95,927,497 , GRCh37.p13 chr5: 94,717,388-95,263,201 SKIC3, ARSK, 17 more genes
    nsv6405135copy number variation1nstd223human GRCh38 chr5: 95,768,680-95,951,039 , GRCh37.p13 chr5: 95,104,384-95,286,743 LOC105379091, LINC01554, 6 more genes
    nsv6400634copy number variation1nstd223human GRCh38 chr5: 95,706,601-95,712,200 , GRCh37.p13 chr5: 95,042,305-95,047,904 RHOBTB3, SPATA9
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
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