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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
    nsv7097303copy number variation1nstd102humanPathogenic GRCh37 chr5: 95,998,127-96,107,383 , GRCh38.p12 chr5: 96,662,423-96,771,679 CAST, ERAP1, 1 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
    nsv7056329inversion1nstd229human GRCh38 chr5: 96,758,696-96,771,689 , GRCh37.p13 chr5: 96,094,400-96,107,393 ERAP1, CAST
    nsv7055396inversion1nstd229human GRCh38 chr5: 96,167,047-97,983,533 , GRCh37.p13 chr5: 95,502,751-97,319,237 MTCYBP40, LINC02234, 22 more genes
    nsv7047849inversion1nstd229human GRCh38 chr5: 96,757,688-96,824,430 , GRCh37.p13 chr5: 96,093,392-96,160,133 ERAP1, CAST
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv6773874copy number variation1nstd229human GRCh38 chr5: 96,745,135-96,795,328 , GRCh37.p13 chr5: 96,080,839-96,131,031 CAST, ERAP1
    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
    nsv6772411copy number variation1nstd229human GRCh38 chr5: 96,306,242-96,783,194 , GRCh37.p13 chr5: 95,641,946-96,118,898 CAST, LOC107986363, 5 more genes
    nsv6772251copy number variation1nstd229human GRCh38 chr5: 96,326,801-96,820,500 , GRCh37.p13 chr5: 95,662,505-96,156,203 CAST, PCSK1, 5 more genes
    nsv6771293copy number variation1nstd229human GRCh38 chr5: 96,760,217-96,768,401 , GRCh37.p13 chr5: 96,095,921-96,104,105 CAST, ERAP1
    nsv6770382copy number variation1nstd229human GRCh38 chr5: 96,696,906-96,700,299 , GRCh37.p13 chr5: 96,032,610-96,036,003 CAST
    nsv6769882copy number variation1nstd229human GRCh38 chr5: 96,671,797-96,680,777 , GRCh37.p13 chr5: 96,007,501-96,016,481 CAST
    nsv6769045copy number variation1nstd229human GRCh38 chr5: 96,668,779-96,672,010 , GRCh37.p13 chr5: 96,004,483-96,007,714 CAST
    nsv6768707copy number variation1nstd229human GRCh38 chr5: 96,742,559-96,744,557 , GRCh37.p13 chr5: 96,078,263-96,080,261 CAST
    nsv6768538copy number variation1nstd229human GRCh38 chr5: 96,650,784-96,744,561 , GRCh37.p13 chr5: 95,986,488-96,080,265 CAST, LOC107986363
    nsv6766027copy number variation1nstd229human GRCh38 chr5: 96,761,385-96,817,715 , GRCh37.p13 chr5: 96,097,089-96,153,418 CAST, ERAP1
    nsv6764992copy number variation1nstd229human GRCh38 chr5: 96,713,419-96,724,472 , GRCh37.p13 chr5: 96,049,123-96,060,176 CAST, LOC107986363
    nsv6764774copy number variation1nstd229human GRCh38 chr5: 96,692,910-96,694,796 , GRCh37.p13 chr5: 96,028,614-96,030,500 CAST
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