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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973642insertion1nstd209human GRCh38 chr14: 76,029,868-76,029,868 , GRCh37.p13 chr14: 76,496,211-76,496,211 IFT43
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5725375mobile element insertion1nstd211human GRCh38 chr14: 76,062,753-76,062,753 , GRCh37.p13 chr14: 76,529,096-76,529,096 IFT43
    nsv5706867mobile element insertion2nstd211human GRCh38 chr14: 76,078,547-76,078,547 , GRCh37.p13 chr14: 76,544,890-76,544,890 IFT43, LOC105370573
    nsv5705356mobile element insertion1nstd211human GRCh38 chr14: 76,014,106-76,014,106 , GRCh37.p13 chr14: 76,480,449-76,480,449 IFT43, LOC100506576
    nsv5512933copy number variation1nstd206human GRCh38 chr14: 76,025,243-76,025,314 , GRCh37.p13 chr14: 76,491,586-76,491,657 IFT43
    nsv5503760copy number variation1nstd206human GRCh38 chr14: 76,062,641-76,073,195 , GRCh37.p13 chr14: 76,528,984-76,539,538 IFT43
    nsv5496283copy number variation1nstd206human GRCh38 chr14: 76,071,813-76,073,181 , GRCh37.p13 chr14: 76,538,156-76,539,524 IFT43
    nsv5433878mobile element insertion1nstd206human GRCh38 chr14: 76,014,106-76,014,157 , GRCh37.p13 chr14: 76,480,449-76,480,500 IFT43, LOC100506576
    nsv5428088mobile element insertion1nstd206human GRCh38 chr14: 76,014,106-76,014,129 , GRCh37.p13 chr14: 76,480,449-76,480,472 LOC100506576, IFT43
    nsv5417066mobile element insertion1nstd206human GRCh38 chr14: 76,078,547-76,078,572 , GRCh37.p13 chr14: 76,544,890-76,544,915 IFT43, LOC105370573
    nsv5357406translocation1nstd200human GRCh38 chr14: 76,071,812-76,071,812 , GRCh38 chr14: 76,073,181-76,073,181 , GRCh37.p13 chr14: 76,539,524-76,539,524 , GRCh37.p13 chr14: 76,538,155-76,538,155 IFT43
    nsv5345725translocation1nstd200human GRCh37 chr1: 244,561,124-244,561,124 , GRCh37 chr14: 76,496,237-76,496,237 , GRCh38.p12 chr1: 244,397,822-244,397,822 , GRCh38.p12 chr14: 76,029,894-76,029,894 IFT43
    nsv5338769translocation1nstd200human GRCh37 chr14: 76,508,734-76,508,734 , GRCh37 chr14: 76,508,825-76,508,825 , GRCh38.p12 chr14: 76,042,482-76,042,482 , GRCh38.p12 chr14: 76,042,391-76,042,391 IFT43
    nsv5331545translocation1nstd200human GRCh37 chr14: 76,538,156-76,538,156 , GRCh37 chr14: 76,539,524-76,539,524 , GRCh38.p12 chr14: 76,071,813-76,071,813 , GRCh38.p12 chr14: 76,073,181-76,073,181 IFT43
    nsv5315695copy number variation1nstd204human GRCh38.p13 chr14: 76,071,812-76,073,181 , GRCh37.p13 chr14: 76,538,155-76,539,524 IFT43
    nsv5267164copy number variation1nstd204human GRCh38.p13 chr14: 76,071,467-76,073,216 , GRCh37.p13 chr14: 76,537,810-76,539,559 IFT43
    nsv5144612mobile element insertion1nstd203human GRCh38 chr14: 75,998,524-75,998,538 , GRCh37.p13 chr14: 76,464,867-76,464,881 IFT43
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5000128copy number variation1nstd200human GRCh38 chr14: 76,042,391-76,042,482 , GRCh37.p13 chr14: 76,508,734-76,508,825 IFT43
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