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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097148copy number variation1nstd102humanPathogenic GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680 RPL37P25, CCNO, 69 more genes
    nsv7057901inversion1nstd229human GRCh38 chr5: 53,201,194-56,162,991 , GRCh37.p13 chr5: 52,497,024-55,458,818 , PLPP1, 55 more genes
    nsv7057158inversion1nstd229human GRCh38 chr5: 54,567,766-54,571,236 , GRCh37.p13 chr5: 53,863,596-53,867,066 SNX18
    nsv7056130inversion1nstd229human GRCh38 chr5: 53,218,622-56,162,980 , GRCh37.p13 chr5: 52,514,452-55,458,807 , ASS1P9, 54 more genes
    nsv7052227inversion1nstd229human GRCh38 chr5: 54,567,610-54,574,675 , GRCh37.p13 chr5: 53,863,440-53,870,505 SNX18
    nsv7042506inversion1nstd229human GRCh38 chr5: 54,605,093-54,605,172 , GRCh37.p13 chr5: 53,900,923-53,901,002 SNX18
    nsv6777453copy number variation1nstd229human GRCh38 chr5: 54,610,081-54,628,599 , GRCh37.p13 chr5: 53,905,911-53,924,429 SNX18
    nsv6776049copy number variation1nstd229human GRCh38 chr5: 54,206,978-54,565,421 , GRCh37.p13 chr5: 53,502,808-53,861,251 LINC01033, RPL37P25, 3 more genes
    nsv6773259copy number variation1nstd229human GRCh38 chr5: 54,575,340-54,593,691 , GRCh37.p13 chr5: 53,871,170-53,889,521 SNX18
    nsv6769759copy number variation1nstd229human GRCh38 chr5: 54,520,522-54,524,455 , GRCh37.p13 chr5: 53,816,352-53,820,285 SNX18
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6766281copy number variation1nstd229human GRCh38 chr5: 54,596,901-54,601,900 , GRCh37.p13 chr5: 53,892,731-53,897,730 SNX18
    nsv6764700copy number variation1nstd229human GRCh38 chr5: 54,538,126-54,538,459 , GRCh37.p13 chr5: 53,833,956-53,834,289 SNX18
    nsv6764484copy number variation1nstd229human GRCh38 chr5: 54,569,748-54,569,935 , GRCh37.p13 chr5: 53,865,578-53,865,765 SNX18
    nsv6760687copy number variation1nstd229human GRCh38 chr5: 54,559,501-54,576,500 , GRCh37.p13 chr5: 53,855,331-53,872,330 SNX18
    nsv6630543copy number variation2nstd224human GRCh37 chr5: 53,314,757-53,815,658 , GRCh38.p12 chr5: 54,018,927-54,519,828 HSPB3, ARL15, 4 more genes
    nsv6557014inversion1nstd223human GRCh38 chr5: 54,510,591-54,647,487 , GRCh37.p13 chr5: 53,806,421-53,943,316 SNX18
    nsv6412104copy number variation1nstd223human GRCh38 chr5: 54,571,201-54,574,600 , GRCh37.p13 chr5: 53,867,031-53,870,430 SNX18
    nsv6409512copy number variation1nstd223human GRCh38 chr5: 54,206,978-54,565,421 , GRCh37.p13 chr5: 53,502,808-53,861,251 LINC01033, RPL37P25, 3 more genes
    nsv6407569copy number variation1nstd223human GRCh38 chr5: 54,534,612-54,534,719 , GRCh37.p13 chr5: 53,830,442-53,830,549 SNX18
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