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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5970718inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 969,999-970,872 , GRCh38 chr7: 73,440,763-73,441,636 , GRCh37.p13 chr7: 72,855,093-72,855,966 BAZ1B
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5908130copy number variation1nstd209human GRCh38 chr7: 73,496,942-73,497,205 , GRCh37.p13 chr7|NW_003871064.1: 1,026,178-1,026,441 , GRCh37.p13 chr7: 72,911,272-72,911,535 BAZ1B
    nsv5860095copy number variation1nstd209human GRCh38 chr7: 73,492,323-73,495,172 , GRCh37.p13 chr7: 72,906,653-72,909,502 , GRCh37.p13 chr7|NW_003871064.1: 1,021,559-1,024,408 BAZ1B
    nsv5853530copy number variation1nstd209human GRCh38 chr7: 73,464,851-73,466,750 , GRCh37.p13 chr7: 72,879,181-72,881,080 , GRCh37.p13 chr7|NW_003871064.1: 994,087-995,986 BAZ1B
    nsv5686378mobile element insertion2nstd211human GRCh38 chr7: 73,479,109-73,479,109 , GRCh37.p13 chr7: 72,893,439-72,893,439 , GRCh37.p13 chr7|NW_003871064.1: 1,008,345-1,008,345 BAZ1B
    nsv5681674mobile element insertion1nstd211human GRCh38 chr7: 73,458,232-73,458,232 , GRCh37.p13 chr7|NW_003871064.1: 987,468-987,468 , GRCh37.p13 chr7: 72,872,562-72,872,562 BAZ1B
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5476094copy number variation1nstd206human GRCh38 chr7: 73,444,796-73,445,599 , GRCh37.p13 chr7: 72,859,126-72,859,929 , GRCh37.p13 chr7|NW_003871064.1: 974,032-974,835 BAZ1B
    nsv5475998copy number variation1nstd206human GRCh38 chr7: 73,493,340-73,495,207 , GRCh37.p13 chr7: 72,907,670-72,909,537 , GRCh37.p13 chr7|NW_003871064.1: 1,022,576-1,024,443 BAZ1B
    nsv5474248copy number variation1nstd206human GRCh38 chr7: 73,467,107-73,467,588 , GRCh37.p13 chr7: 72,881,437-72,881,918 , GRCh37.p13 chr7|NW_003871064.1: 996,343-996,824 BAZ1B
    nsv5409869mobile element insertion1nstd206human GRCh38 chr7: 73,479,109-73,479,160 , GRCh37.p13 chr7|NW_003871064.1: 1,008,345-1,008,396 , GRCh37.p13 chr7: 72,893,439-72,893,490 BAZ1B
    nsv5404258mobile element insertion1nstd206human GRCh38 chr7: 73,458,232-73,458,283 , GRCh37.p13 chr7|NW_003871064.1: 987,468-987,519 , GRCh37.p13 chr7: 72,872,562-72,872,613 BAZ1B
    nsv5381761copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 71,847,968-73,391,310 , GRCh38.p12 chr7: 72,382,983-73,976,980 CLDN4, CLDN3, 46 more genes
    nsv5186036mobile element insertion1nstd203human GRCh38 chr7: 73,451,904-73,451,921 , GRCh37.p13 chr7|NW_003871064.1: 981,140-981,157 , GRCh37.p13 chr7: 72,866,234-72,866,251 BAZ1B
    nsv5112432mobile element insertion1nstd203human GRCh38 chr7: 73,479,096-73,479,109 , GRCh37.p13 chr7|NW_003871064.1: 1,008,332-1,008,345 , GRCh37.p13 chr7: 72,893,426-72,893,439 BAZ1B
    nsv5112107mobile element insertion1nstd203human GRCh38 chr7: 73,511,721-73,511,735 , GRCh37.p13 chr7|NW_003871064.1: 1,040,957-1,040,971 , GRCh37.p13 chr7: 72,926,051-72,926,065 BAZ1B
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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