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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7067026inversion1nstd229human GRCh38 chr8: 131,472,365-131,932,716 , GRCh37.p13 chr8: 132,484,612-132,944,963 EFR3A, LOC100420215, 1 more genes
    nsv7062365inversion1nstd229human GRCh38 chr8: 131,355,985-132,586,379 , GRCh37.p13 chr8: 132,368,232-133,598,626 EFR3A, HHLA1, 8 more genes
    nsv7061330inversion1nstd229human GRCh38 chr8: 131,942,747-131,950,550 , GRCh37.p13 chr8: 132,954,994-132,962,797 EFR3A
    nsv7058703inversion1nstd229human GRCh38 chr8: 131,875,230-131,963,564 , GRCh37.p13 chr8: 132,887,477-132,975,811 EFR3A, LOC107986976
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6855529copy number variation1nstd229human GRCh38 chr8: 131,914,560-132,108,225 , GRCh37.p13 chr8: 132,926,807-133,120,472 OC90, HHLA1, 1 more genes
    nsv6853439copy number variation1nstd229human GRCh38 chr8: 131,919,845-131,923,683 , GRCh37.p13 chr8: 132,932,092-132,935,930 EFR3A
    nsv6852987copy number variation1nstd229human GRCh38 chr8: 131,982,157-131,982,194 , GRCh37.p13 chr8: 132,994,404-132,994,441 EFR3A
    nsv6850094copy number variation1nstd229human GRCh38 chr8: 131,971,299-131,973,887 , GRCh37.p13 chr8: 132,983,546-132,986,134 EFR3A
    nsv6850062copy number variation1nstd229human GRCh38 chr8: 131,928,639-131,937,179 , GRCh37.p13 chr8: 132,940,886-132,949,426 EFR3A
    nsv6848910copy number variation1nstd229human GRCh38 chr8: 131,916,518-131,916,628 , GRCh37.p13 chr8: 132,928,765-132,928,875 EFR3A
    nsv6848076copy number variation1nstd229human GRCh38 chr8: 131,928,116-131,928,244 , GRCh37.p13 chr8: 132,940,363-132,940,491 EFR3A
    nsv6846597copy number variation1nstd229human GRCh38 chr8: 131,798,565-132,239,874 , GRCh37.p13 chr8: 132,810,812-133,252,121 OC90, EFR3A, 3 more genes
    nsv6846409copy number variation1nstd229human GRCh38 chr8: 132,008,343-132,008,440 , GRCh37.p13 chr8: 133,020,590-133,020,687 EFR3A
    nsv6845424copy number variation1nstd229human GRCh38 chr8: 131,567,446-132,158,530 , GRCh37.p13 chr8: 132,579,693-133,170,777 LOC100420215, LOC107986976, 4 more genes
    nsv6845224copy number variation1nstd229human GRCh38 chr8: 132,000,667-132,000,762 , GRCh37.p13 chr8: 133,012,914-133,013,009 EFR3A
    nsv6844360copy number variation1nstd229human GRCh38 chr8: 131,957,713-132,392,691 , GRCh37.p13 chr8: 132,969,960-133,404,938 HHLA1, KCNQ3, 2 more genes
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