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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147161insertion1nstd232human GRCh37.p13 chr2: 3,504,765-3,504,765 , GRCh38.p12 chr2: 3,500,994-3,500,994 , GRCh38.p12 chr2|NT_187522.1: 110,464-110,464 ADI1
    nsv7138204copy number variation1nstd232human GRCh37.p13 chr2: 3,490,505-3,490,558 , GRCh38.p12 chr2: 3,486,734-3,486,787 , GRCh38.p12 chr2|NT_187522.1: 96,204-96,257 0
    nsv7137596insertion1nstd232human GRCh37.p13 chr2: 3,447,662-3,447,662 , GRCh38.p12 chr2: 3,443,891-3,443,891 , GRCh38.p12 chr2|NT_187522.1: 53,360-53,360 TRAPPC12
    nsv7096158copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,391,395-3,624,240 , GRCh38.p12 chr2: 3,387,624-3,576,650 , GRCh38.p12 chr2|NT_187522.1: 1-120,616 RPS7, RNASEH1-DT, 4 more genes
    nsv7096157copy number variation1nstd102humanPathogenic GRCh37 chr2: 3,391,395-3,428,454 , GRCh38.p12 chr2: 3,387,624-3,424,683 , GRCh38.p12 chr2|NT_187522.1: 1-34,747 TRAPPC12
    nsv6290360copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,432,176-3,504,178 , GRCh38.p12 chr2: 3,428,405-3,500,407 , GRCh38.p12 chr2|NT_187522.1: 38,469-109,877 ADI1, TRAPPC12, 1 more genes
    nsv4788238copy number variation1nstd200human GRCh37 chr2: 3,334,536-3,460,285 , GRCh38.p12 chr2: 3,330,765-3,456,514 , GRCh38.p12 chr2|NT_187522.1: 1-65,984 EIPR1, TRAPPC12
    nsv4769992copy number variation1nstd200human GRCh37 chr2: 3,498,492-3,499,531 , GRCh38.p12 chr2: 3,494,721-3,495,760 , GRCh38.p12 chr2|NT_187522.1: 104,191-105,230 ADI1
    nsv4769991copy number variation1nstd200human GRCh37 chr2: 3,445,409-3,445,476 , GRCh38.p12 chr2|NT_187522.1: 51,140-51,207 , GRCh38.p12 chr2: 3,441,638-3,441,705 TRAPPC12
    nsv4764329insertion1nstd199human GRCh37 chr2: 3,443,321-3,443,321 , GRCh38.p12 chr2: 3,439,550-3,439,550 , GRCh38.p12 chr2|NT_187522.1: 49,052-49,052 TRAPPC12
    nsv4757417insertion1nstd199human GRCh37 chr2: 3,452,398-3,452,398 , GRCh38.p12 chr2: 3,448,627-3,448,627 , GRCh38.p12 chr2|NT_187522.1: 58,097-58,097 TRAPPC12
    nsv4756145insertion1nstd199human GRCh37 chr2: 3,458,212-3,458,212 , GRCh38.p12 chr2|NT_187522.1: 63,911-63,911 , GRCh38.p12 chr2: 3,454,441-3,454,441 TRAPPC12
    nsv4745540copy number variation1nstd199human GRCh37 chr2: 3,490,493-3,490,549 , GRCh38.p12 chr2: 3,486,722-3,486,778 , GRCh38.p12 chr2|NT_187522.1: 96,192-96,248 0
    nsv4720094insertion1nstd186human GRCh37 chr2: 3,479,246-3,479,246 , GRCh38.p12 chr2: 3,475,475-3,475,475 , GRCh38.p12 chr2|NT_187522.1: 84,945-84,945 TRAPPC12
    nsv4689020mobile element insertion1nstd186human GRCh37 chr2: 3,479,246-3,479,246 , GRCh38.p12 chr2: 3,475,475-3,475,475 , GRCh38.p12 chr2|NT_187522.1: 84,945-84,945 TRAPPC12
    nsv4674765copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,425,359-3,504,178 , GRCh38.p12 chr2: 3,421,588-3,500,407 , GRCh38.p12 chr2|NT_187522.1: 31,648-109,877 TRAPPC12, LOC112268321, 1 more genes
    nsv4595517copy number variation1nstd183human GRCh37 chr2: 3,469,313-3,470,256 , GRCh38.p12 chr2: 3,465,542-3,466,485 , GRCh38.p12 chr2|NT_187522.1: 75,012-75,955 TRAPPC12
    nsv4585841copy number variation2nstd183human GRCh37 chr2: 3,440,426-3,442,218 , GRCh38.p12 chr2|NT_187522.1: 46,719-47,999 , GRCh38.p12 chr2: 3,436,655-3,438,447 TRAPPC12
    nsv4537679insertion1nstd166human GRCh37.p13 chr2: 3,479,246-3,479,246 , GRCh38.p12 chr2|NT_187522.1: 84,945-84,945 , GRCh38.p12 chr2: 3,475,475-3,475,475 TRAPPC12
    nsv4466835mobile element insertion1nstd166human GRCh37.p13 chr2: 3,427,555-3,427,555 , GRCh38.p12 chr2: 3,423,784-3,423,784 , GRCh38.p12 chr2|NT_187522.1: 33,848-33,848 TRAPPC12
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