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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094072copy number variation1nstd102humanUncertain significance GRCh37 chr13: 31,033,232-33,638,323 , GRCh38.p12 chr13: 30,459,095-33,064,186 N4BP2L2, RNY1P4, 37 more genes
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6937886copy number variation1nstd229human GRCh38 chr13: 30,491,524-30,492,530 , GRCh37.p13 chr13: 31,065,661-31,066,667 HMGB1
    nsv6936193copy number variation1nstd229human GRCh38 chr13: 30,605,466-30,615,599 , GRCh37.p13 chr13: 31,179,603-31,189,736 HMGB1
    nsv6936084copy number variation1nstd229human GRCh38 chr13: 30,601,463-30,601,783 , GRCh37.p13 chr13: 31,175,600-31,175,920 HMGB1
    nsv6935628copy number variation1nstd229human GRCh38 chr13: 30,469,466-30,469,687 , GRCh37.p13 chr13: 31,043,603-31,043,824 HMGB1
    nsv6929769copy number variation1nstd229human GRCh38 chr13: 30,489,041-30,489,191 , GRCh37.p13 chr13: 31,063,178-31,063,328 HMGB1
    nsv6929254copy number variation1nstd229human GRCh38 chr13: 30,465,901-30,937,900 , GRCh37.p13 chr13: 31,040,038-31,512,037 HMGB1, TRN-GTT2-4, 10 more genes
    nsv6928056copy number variation1nstd229human GRCh38 chr13: 30,505,431-30,505,564 , GRCh37.p13 chr13: 31,079,568-31,079,701 HMGB1
    nsv6927775copy number variation1nstd229human GRCh38 chr13: 30,476,703-30,573,747 , GRCh37.p13 chr13: 31,050,840-31,147,884 HMGB1, PTPN2P2, 2 more genes
    nsv6926548copy number variation1nstd229human GRCh38 chr13: 30,467,208-30,477,487 , GRCh37.p13 chr13: 31,041,345-31,051,624 HMGB1
    nsv6925835copy number variation1nstd229human GRCh38 chr13: 30,509,287-30,519,650 , GRCh37.p13 chr13: 31,083,424-31,093,787 HMGB1
    nsv6924817copy number variation1nstd229human GRCh38 chr13: 30,609,000-30,609,045 , GRCh37.p13 chr13: 31,183,137-31,183,182 HMGB1
    nsv6924639copy number variation1nstd229human GRCh38 chr13: 30,472,063-30,474,347 , GRCh37.p13 chr13: 31,046,200-31,048,484 HMGB1
    nsv6923917copy number variation1nstd229human GRCh38 chr13: 30,612,160-30,612,228 , GRCh37.p13 chr13: 31,186,297-31,186,365 HMGB1
    nsv6920278copy number variation1nstd229human GRCh38 chr13: 30,553,155-30,557,369 , GRCh37.p13 chr13: 31,127,292-31,131,506 HMGB1, PTPN2P2
    nsv6918657copy number variation1nstd229human GRCh38 chr13: 30,367,401-30,509,500 , GRCh37.p13 chr13: 30,941,538-31,083,637 LINC00426, HMGB1, 3 more genes
    nsv6918519copy number variation1nstd229human GRCh38 chr13: 30,508,425-30,610,463 , GRCh37.p13 chr13: 31,082,562-31,184,600 HMGB1, RBM22P2, 2 more genes
    nsv6918120copy number variation1nstd229human GRCh38 chr13: 30,389,860-30,459,944 , GRCh37.p13 chr13: 30,963,997-31,034,081 HMGB1, LINC01058, 2 more genes
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