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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7146526copy number variation1nstd232human GRCh37.p13 chr5: 262,320-262,413 , GRCh38.p12 chr5: 262,205-262,298 SDHA
    nsv7143466copy number variation1nstd232human GRCh37.p13 chr5: 260,927-260,990 , GRCh38.p12 chr5: 260,812-260,875 SDHA
    nsv7141901insertion1nstd232human GRCh37.p13 chr5: 228,448-228,448 , GRCh38.p12 chr5: 228,333-228,333 SDHA
    nsv7141827copy number variation1nstd232human GRCh37.p13 chr5: 261,825-261,953 , GRCh38.p12 chr5: 261,710-261,838 SDHA
    nsv7139234insertion1nstd232human GRCh37.p13 chr5: 224,637-224,637 , GRCh38.p12 chr5: 224,522-224,522 SDHA
    nsv7137451insertion1nstd232human GRCh37.p13 chr5: 225,676-225,676 , GRCh38.p12 chr5: 225,561-225,561 SDHA
    nsv7136980copy number variation1nstd102humanUncertain significance GRCh37 chr5: 233,694-233,695 , GRCh38 chr5: 233,579-233,580 SDHA
    nsv7136971copy number variation1nstd102humanUncertain significance GRCh37 chr5: 218,337-257,198 , GRCh38.p12 chr5: 218,222-257,083 SDHA, CCDC127
    nsv7136965copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 218,337-236,542 , GRCh38.p12 chr5: 218,222-236,427 SDHA, CCDC127
    nsv7093260copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 228,446-228,524 , GRCh38 chr5: 228,331-228,409 SDHA
    nsv7053030inversion1nstd229human GRCh38 chr5: 244,583-250,819 , GRCh37.p13 chr5: 244,698-250,934 SDHA
    nsv7047634inversion1nstd229human GRCh38 chr5: 90,743-229,045 , GRCh37.p13 chr5: 90,858-229,160 CCDC127, LRRC14B, 2 more genes
    nsv7045728inversion1nstd229human GRCh38 chr5: 182,184-229,696 , GRCh37.p13 chr5: 182,299-229,811 CCDC127, LRRC14B, 2 more genes
    nsv7042837inversion1nstd229human GRCh38 chr5: 240,710-251,025 , GRCh37.p13 chr5: 240,825-251,140 SDHA
    nsv7042391inversion1nstd229human GRCh38 chr5: 190,811-661,964 , GRCh37.p13 chr5: 190,926-662,079 LOC100310782, LOC105374606, 20 more genes
    nsv6777276copy number variation1nstd229human GRCh38 chr5: 246,176-256,623 , GRCh37.p13 chr5: 246,291-256,738 SDHA
    nsv6776249copy number variation1nstd229human GRCh38 chr5: 191,265-303,477 , GRCh37.p13 chr5: 191,380-303,592 CCDC127, LRRC14B, 5 more genes
    nsv6774693copy number variation1nstd229human GRCh38 chr5: 231,718-232,743 , GRCh37.p13 chr5: 231,833-232,858 SDHA
    nsv6774279copy number variation1nstd229human GRCh38 chr5: 223,897-231,208 , GRCh37.p13 chr5: 224,012-231,323 SDHA
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