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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5906269copy number variation1nstd209human GRCh38 chr5: 37,143,762-37,144,235 , GRCh37.p13 chr5: 37,143,864-37,144,337 CPLANE1
    nsv5890834copy number variation1nstd209human GRCh38 chr5: 37,124,118-37,199,674 , GRCh37.p13 chr5: 37,124,220-37,199,776 CPLANE1, RBISP2
    nsv5888994copy number variation1nstd209human GRCh38 chr5: 37,191,488-37,192,679 , GRCh37.p13 chr5: 37,191,590-37,192,781 CPLANE1
    nsv5843031copy number variation1nstd209human GRCh38 chr5: 37,194,867-37,199,399 , GRCh37.p13 chr5: 37,194,969-37,199,501 CPLANE1
    nsv5842707copy number variation1nstd209human GRCh38 chr5: 37,170,961-37,173,300 , GRCh37.p13 chr5: 37,171,063-37,173,402 CPLANE1
    nsv5842404copy number variation1nstd209human GRCh38 chr5: 37,124,070-37,137,487 , GRCh37.p13 chr5: 37,124,172-37,137,589 CPLANE1, RBISP2
    nsv5684437mobile element insertion2nstd211human GRCh38 chr5: 37,069,367-37,069,367 , GRCh37.p13 chr5: 37,069,469-37,069,469 CPLANE1
    nsv5676123mobile element insertion1nstd211human GRCh38 chr5: 37,082,781-37,082,781 , GRCh37.p13 chr5: 37,082,883-37,082,883 CPLANE1
    nsv5676004mobile element insertion2nstd211human GRCh38 chr5: 37,201,295-37,201,295 , GRCh37.p13 chr5: 37,201,397-37,201,397 CPLANE1
    nsv5673664copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,953,799-37,064,994 , GRCh38.p12 chr5: 36,953,697-37,064,892 NIPBL, CPLANE1
    nsv5673575copy number variation1nstd102humanPathogenic GRCh38 chr5: 37,120,202-37,120,280 , GRCh37 chr5: 37,120,304-37,120,382 CPLANE1
    nsv5564200copy number variation1nstd102humanUncertain significance GRCh37 chr5: 37,107,684-37,247,820 , GRCh38.p12 chr5: 37,107,582-37,247,718 OFD1P17, CPLANE1-AS1, 3 more genes
    nsv5540302insertion1nstd206human GRCh38 chr5: 37,069,364-37,069,381 , GRCh37.p13 chr5: 37,069,466-37,069,483 CPLANE1
    nsv5473159copy number variation1nstd206human GRCh38 chr5: 37,159,075-37,159,181 , GRCh37.p13 chr5: 37,159,177-37,159,283 CPLANE1
    nsv5472119copy number variation1nstd206human GRCh38 chr5: 37,072,425-37,072,573 , GRCh37.p13 chr5: 37,072,527-37,072,675 CPLANE1
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5468920copy number variation1nstd206human GRCh38 chr5: 37,145,372-37,511,030 , GRCh37.p13 chr5: 37,145,474-37,511,132 NUP155, OFD1P17, 6 more genes
    nsv5467132copy number variation1nstd206human GRCh38 chr5: 37,191,521-37,192,680 , GRCh37.p13 chr5: 37,191,623-37,192,782 CPLANE1
    nsv5464795copy number variation1nstd206human GRCh38 chr5: 37,182,548-37,218,548 , GRCh37.p13 chr5: 37,182,650-37,218,650 CPLANE1, OFD1P17
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