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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952414insertion1nstd209human GRCh38 chr9: 105,533,416-105,533,416 , GRCh37.p13 chr9: 108,295,697-108,295,697 FSD1L
    nsv5920777copy number variation1nstd209human GRCh38 chr9: 105,551,356-105,551,598 , GRCh37.p13 chr9: 108,313,637-108,313,879 FSD1L
    nsv5919775copy number variation1nstd209human GRCh38 chr9: 105,485,999-105,486,059 , GRCh37.p13 chr9: 108,248,280-108,248,340 FSD1L
    nsv5910217copy number variation1nstd209human GRCh38 chr9: 105,477,079-105,478,286 , GRCh37.p13 chr9: 108,239,360-108,240,567 FSD1L
    nsv5857087copy number variation1nstd209human GRCh38 chr9: 105,477,271-105,478,270 , GRCh37.p13 chr9: 108,239,552-108,240,551 FSD1L
    nsv5701841mobile element insertion1nstd211human GRCh38 chr9: 105,481,204-105,481,204 , GRCh37.p13 chr9: 108,243,485-108,243,485 FSD1L
    nsv5700877mobile element insertion2nstd211human GRCh38 chr9: 105,525,792-105,525,792 , GRCh37.p13 chr9: 108,288,073-108,288,073 RALGAPA1P1, FSD1L
    nsv5699654mobile element insertion1nstd211human GRCh38 chr9: 105,485,556-105,485,556 , GRCh37.p13 chr9: 108,247,837-108,247,837 FSD1L
    nsv5594937copy number variation1nstd207human GRCh38 chr9: 105,485,999-105,486,059 , GRCh37.p13 chr9: 108,248,280-108,248,340 FSD1L
    nsv5491752copy number variation1nstd206human GRCh38 chr9: 105,486,001-105,486,060 , GRCh37.p13 chr9: 108,248,282-108,248,341 FSD1L
    nsv5483429copy number variation1nstd206human GRCh38 chr9: 105,440,933-105,442,690 , GRCh37.p13 chr9: 108,203,214-108,204,971 FSD1L
    nsv5477325copy number variation1nstd206human GRCh38 chr9: 105,491,387-105,494,387 , GRCh37.p13 chr9: 108,253,668-108,256,668 FSD1L
    nsv5411484mobile element insertion1nstd206human GRCh38 chr9: 105,525,792-105,525,843 , GRCh37.p13 chr9: 108,288,073-108,288,124 RALGAPA1P1, FSD1L
    nsv5345551translocation1nstd200human GRCh37 chr9: 108,313,640-108,313,640 , GRCh37 chr9: 108,313,880-108,313,880 , GRCh38.p12 chr9: 105,551,599-105,551,599 , GRCh38.p12 chr9: 105,551,359-105,551,359 FSD1L
    nsv5317653copy number variation1nstd204human GRCh38.p13 chr9: 105,531,039-105,538,295 , GRCh37.p13 chr9: 108,293,320-108,300,576 FSD1L
    nsv5256112copy number variation1nstd204human GRCh38.p13 chr9: 105,545,201-105,545,500 , GRCh37.p13 chr9: 108,307,482-108,307,781 FSD1L
    nsv5251896copy number variation1nstd204human GRCh38.p13 chr9: 105,520,304-105,522,319 , GRCh37.p13 chr9: 108,282,585-108,284,600 FSD1L, RALGAPA1P1
    nsv5248044copy number variation1nstd204human GRCh38.p13 chr9: 105,531,101-105,538,300 , GRCh37.p13 chr9: 108,293,382-108,300,581 FSD1L
    nsv5241921copy number variation1nstd204human GRCh38.p13 chr9: 105,530,891-105,538,403 , GRCh37.p13 chr9: 108,293,172-108,300,684 FSD1L
    nsv5129832mobile element insertion1nstd203human GRCh38 chr9: 105,531,040-105,531,055 , GRCh37.p13 chr9: 108,293,321-108,293,336 FSD1L
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