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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7052624inversion1nstd229human GRCh38 chr2: 218,630,247-218,630,317 , GRCh37.p13 chr2: 219,494,970-219,495,040 PLCD4
    nsv7048316inversion1nstd229human GRCh38 chr2: 217,690,925-222,070,373 , GRCh37.p13 chr2: 218,555,648-222,935,092 LOC105373895, CXCR2P1, 119 more genes
    nsv6696943copy number variation1nstd229human GRCh38 chr2: 218,598,094-218,611,851 , GRCh37.p13 chr2: 219,462,817-219,476,574 PLCD4
    nsv6696116copy number variation1nstd229human GRCh38 chr2: 218,605,248-218,621,140 , GRCh37.p13 chr2: 219,469,971-219,485,863 PLCD4
    nsv6692278copy number variation1nstd229human GRCh38 chr2: 218,624,073-218,627,719 , GRCh37.p13 chr2: 219,488,796-219,492,442 PLCD4, TRQ-CTG16-1
    nsv6690102copy number variation1nstd229human GRCh38 chr2: 218,455,001-218,684,900 , GRCh37.p13 chr2: 219,319,724-219,549,623 USP37, CNOT9, 8 more genes
    nsv6685864copy number variation1nstd229human GRCh38 chr2: 216,932,763-218,687,760 , GRCh37.p13 chr2: 217,797,486-219,552,483 LOC105373872, IGFBP-AS1, 45 more genes
    nsv6685442copy number variation1nstd229human GRCh38 chr2: 218,614,062-218,623,630 , GRCh37.p13 chr2: 219,478,785-219,488,353 PLCD4
    nsv6684942copy number variation1nstd229human GRCh38 chr2: 218,629,346-218,639,590 , GRCh37.p13 chr2: 219,494,069-219,504,313 ZNF142, PLCD4
    nsv6681346copy number variation1nstd229human GRCh38 chr2: 218,609,401-218,615,500 , GRCh37.p13 chr2: 219,474,124-219,480,223 PLCD4
    nsv6678680copy number variation1nstd229human GRCh38 chr2: 218,631,543-218,631,620 , GRCh37.p13 chr2: 219,496,266-219,496,343 PLCD4, ZNF142
    nsv6551496inversion1nstd223human GRCh38 chr2: 218,613,079-218,614,091 , GRCh37.p13 chr2: 219,477,802-219,478,814 PLCD4
    nsv6550800inversion1nstd223human GRCh38 chr2: 218,613,166-218,614,189 , GRCh37.p13 chr2: 219,477,889-219,478,912 PLCD4
    nsv6546494inversion1nstd223human GRCh38 chr2: 218,631,191-218,631,740 , GRCh37.p13 chr2: 219,495,914-219,496,463 ZNF142, PLCD4
    nsv6535767inversion1nstd223human GRCh38 chr2: 218,627,018-218,627,630 , GRCh37.p13 chr2: 219,491,741-219,492,353 PLCD4
    nsv6345677copy number variation1nstd223human GRCh38 chr2: 218,624,066-218,627,722 , GRCh37.p13 chr2: 219,488,789-219,492,445 PLCD4, TRQ-CTG16-1
    nsv6339254copy number variation1nstd223human GRCh38 chr2: 218,613,249-218,617,312 , GRCh37.p13 chr2: 219,477,972-219,482,035 PLCD4
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313768copy number variation1nstd102humanUncertain significance GRCh37 chr2: 218,210,665-220,141,650 , GRCh38.p12 chr2: 217,345,942-219,276,928 PNKD, RNU6-136P, 73 more genes
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