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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964214insertion1nstd209human GRCh38 chr9: 128,747,261-128,747,261 , GRCh37.p13 chr9: 131,509,540-131,509,540 ZER1
    nsv5961950insertion1nstd209human GRCh38 chr9: 128,734,144-128,734,144 , GRCh37.p13 chr9: 131,496,423-131,496,423 ZER1
    nsv5910739copy number variation1nstd209human GRCh38 chr9: 128,744,149-128,744,730 , GRCh37.p13 chr9: 131,506,428-131,507,009 ZER1
    nsv5861733copy number variation1nstd209human GRCh38 chr9: 128,757,108-128,760,007 , GRCh37.p13 chr9: 131,519,387-131,522,286 ZER1
    nsv5705573mobile element insertion1nstd211human GRCh38 chr9: 128,763,135-128,763,135 , GRCh37.p13 chr9: 131,525,414-131,525,414 ZER1
    nsv5627352insertion1nstd207human GRCh38 chr9: 128,747,258-128,747,258 , GRCh37.p13 chr9: 131,509,537-131,509,537 ZER1
    nsv5549800insertion1nstd206human GRCh38 chr9: 128,747,260-128,747,263 , GRCh37.p13 chr9: 131,509,539-131,509,542 ZER1
    nsv5490275copy number variation1nstd206human GRCh38 chr9: 128,759,416-128,767,041 , GRCh37.p13 chr9: 131,521,695-131,529,320 ZER1
    nsv5475610copy number variation1nstd206human GRCh38 chr9: 128,744,431-128,744,744 , GRCh37.p13 chr9: 131,506,710-131,507,023 ZER1
    nsv5403817mobile element insertion1nstd206human GRCh38 chr9: 128,763,135-128,763,186 , GRCh37.p13 chr9: 131,525,414-131,525,465 ZER1
    nsv5251878copy number variation1nstd204human GRCh38.p13 chr9: 128,649,801-128,795,400 , GRCh37.p13 chr9: 131,412,080-131,557,679 , DYNC2I2, 9 more genes
    nsv5241889copy number variation1nstd204human GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379 , KYAT1, 32 more genes
    nsv4988410copy number variation1nstd200human GRCh38 chr9: 128,760,492-128,761,814 , GRCh37.p13 chr9: 131,522,771-131,524,093 ZER1
    nsv4988409copy number variation1nstd200human GRCh38 chr9: 128,759,416-128,767,041 , GRCh37.p13 chr9: 131,521,695-131,529,320 ZER1
    nsv4988408copy number variation1nstd200human GRCh38 chr9: 128,743,176-128,747,654 , GRCh37.p13 chr9: 131,505,455-131,509,933 ZER1
    nsv4985749copy number variation1nstd200human GRCh38 chr9: 128,761,676-128,795,458 , GRCh37.p13 chr9: 131,523,955-131,557,737 ZER1, TBC1D13
    nsv4849208copy number variation1nstd200human GRCh37 chr9: 131,505,455-131,509,933 , GRCh38.p12 chr9: 128,743,176-128,747,654 ZER1
    nsv4848429copy number variation1nstd200human GRCh37 chr9: 131,500,711-131,501,211 , GRCh38.p12 chr9: 128,738,432-128,738,932 ZER1
    nsv4845199copy number variation1nstd200human GRCh37 chr9: 131,519,559-131,523,168 , GRCh38.p12 chr9: 128,757,280-128,760,889 ZER1
    nsv4843051copy number variation1nstd200human GRCh37 chr9: 131,521,695-131,529,320 , GRCh38.p12 chr9: 128,759,416-128,767,041 ZER1
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