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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
    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
    nsv5673937copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,150,889-73,604,636 , GRCh38.p12 chr7: 73,736,559-74,190,306 EIF4H, ELN-AS1, 8 more genes
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 more genes
    nsv5631876insertion1nstd207human GRCh38 chr7: 73,861,965-73,861,965 , GRCh37.p13 chr7|NW_003871064.1: 1,391,201-1,391,201 , GRCh37.p13 chr7: 73,276,295-73,276,295 TMEM270
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    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
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4954040copy number variation1nstd200human GRCh38 chr7: 73,823,091-73,911,748 , GRCh37.p13 chr7: 73,237,421-73,326,078 , GRCh37.p13 chr7|NW_003871064.1: 1,352,327-1,440,984 TMEM270, METTL27, 1 more genes
    nsv4769380copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,717,369-74,142,224 , GRCh38.p12 chr7: 73,303,372-74,727,886 CLDN4, MLXIPL, 37 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4730256inversion12nstd198human GRCh38 chr7: 72,909,603-75,903,316 , GRCh37.p13 chr7|NW_003871064.1: 438,839-3,432,552 , CLDN4, 86 more genes
    nsv4729646copy number variation1nstd102humanPathogenic GRCh37 chr7: 68,977,230-73,939,510 , GRCh38.p12 chr7: 69,512,244-74,525,180 LOC105375346, ABHD11-AS1, 70 more genes
    nsv4729135copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,659,674-74,164,894 , GRCh38.p12 chr7: 73,245,641-74,750,557 CLIP2, ABHD11-AS1, 39 more genes
    nsv4728820copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283 FDPSP7, LOC105375352, 119 more genes
    nsv4684125copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,657,228-74,160,300 , GRCh38.p12 chr7: 73,243,195-74,745,961 GTF2I, DNAJC30, 39 more genes
    nsv4675238copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,996,564-73,597,315 , GRCh38.p12 chr7: 73,582,234-74,182,985 RN7SL265P, STX1A, 16 more genes
    nsv4675200copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063 PHB1P15, FKBP6P2, 87 more genes
    nsv4613861copy number variation1nstd183human GRCh37 chr7: 73,227,641-73,457,028 , GRCh38.p12 chr7: 73,813,311-74,042,698 CLDN4, ELN, 2 more genes
    nsv4524713copy number variation1nstd166human GRCh37.p13 chr7: 72,708,999-74,058,000 , GRCh38.p12 chr7: 73,294,999-74,643,669 ELN, LAT2, 35 more genes
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