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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7057534inversion1nstd229human GRCh38 chr3: 172,203,082-172,206,447 , GRCh37.p13 chr3: 171,920,872-171,924,237 FNDC3B
    nsv7057325inversion1nstd229human GRCh38 chr3: 170,134,629-173,143,661 , GRCh37.p13 chr3: 169,852,417-172,861,451 LINC02068, LOC107986052, 45 more genes
    nsv7054784inversion1nstd229human GRCh38 chr3: 172,061,120-172,065,739 , GRCh37.p13 chr3: 171,778,910-171,783,529 FNDC3B
    nsv7050772inversion1nstd229human GRCh38 chr3: 172,197,867-172,203,674 , GRCh37.p13 chr3: 171,915,657-171,921,464 FNDC3B
    nsv7047556inversion1nstd229human GRCh38 chr3: 172,269,386-172,269,467 , GRCh37.p13 chr3: 171,987,176-171,987,257 FNDC3B
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv7044989inversion1nstd229human GRCh38 chr3: 172,151,043-172,154,228 , GRCh37.p13 chr3: 171,868,833-171,872,018 FNDC3B
    nsv6737996copy number variation1nstd229human GRCh38 chr3: 172,380,201-172,425,000 , GRCh37.p13 chr3: 172,097,991-172,142,790 FNDC3B, BZW1P1
    nsv6737968copy number variation1nstd229human GRCh38 chr3: 172,229,617-172,242,659 , GRCh37.p13 chr3: 171,947,407-171,960,449 RN7SL141P, FNDC3B
    nsv6736864copy number variation1nstd229human GRCh38 chr3: 172,044,257-172,044,288 , GRCh37.p13 chr3: 171,762,047-171,762,078 FNDC3B
    nsv6736047copy number variation1nstd229human GRCh38 chr3: 172,264,776-172,267,194 , GRCh37.p13 chr3: 171,982,566-171,984,984 FNDC3B
    nsv6735906copy number variation1nstd229human GRCh38 chr3: 172,238,496-172,244,220 , GRCh37.p13 chr3: 171,956,286-171,962,010 FNDC3B
    nsv6735463copy number variation1nstd229human GRCh38 chr3: 172,090,935-172,091,439 , GRCh37.p13 chr3: 171,808,725-171,809,229 FNDC3B
    nsv6734748copy number variation1nstd229human GRCh38 chr3: 172,056,112-172,058,628 , GRCh37.p13 chr3: 171,773,902-171,776,418 FNDC3B
    nsv6733275copy number variation1nstd229human GRCh38 chr3: 172,063,387-172,073,641 , GRCh37.p13 chr3: 171,781,177-171,791,431 FNDC3B
    nsv6732624copy number variation1nstd229human GRCh38 chr3: 172,375,588-172,375,945 , GRCh37.p13 chr3: 172,093,378-172,093,735 FNDC3B
    nsv6732531copy number variation1nstd229human GRCh38 chr3: 172,139,781-172,253,733 , GRCh37.p13 chr3: 171,857,571-171,971,523 RN7SL141P, FNDC3B, 1 more genes
    nsv6730424copy number variation1nstd229human GRCh38 chr3: 172,043,001-172,043,045 , GRCh37.p13 chr3: 171,760,791-171,760,835 FNDC3B
    nsv6729008copy number variation1nstd229human GRCh38 chr3: 172,355,501-172,359,300 , GRCh37.p13 chr3: 172,073,291-172,077,090 FNDC3B
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