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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5952570insertion1nstd209human GRCh38 chr3: 131,350,923-131,350,923 , GRCh37.p13 chr3: 131,069,767-131,069,767 NUDT16-DT, NEK11
    nsv5904390copy number variation1nstd209human GRCh38 chr3: 131,379,134-131,379,217 , GRCh37.p13 chr3: 131,097,978-131,098,061 NUDT16-DT
    nsv5726865mobile element insertion2nstd211human GRCh38 chr3: 131,350,935-131,350,935 , GRCh37.p13 chr3: 131,069,779-131,069,779 NEK11, NUDT16-DT
    nsv5724531mobile element insertion1nstd211human GRCh38 chr3: 131,338,146-131,338,146 , GRCh37.p13 chr3: 131,056,990-131,056,990 NEK11, NUDT16-DT
    nsv5616159insertion2nstd207human GRCh38 chr3: 131,357,263-131,357,263 , GRCh37.p13 chr3: 131,076,107-131,076,107 NUDT16-DT
    nsv5609095insertion1nstd207human GRCh38 chr3: 131,350,923-131,350,923 , GRCh37.p13 chr3: 131,069,767-131,069,767 NEK11, NUDT16-DT
    nsv5582383copy number variation1nstd207human GRCh38 chr3: 131,379,134-131,379,217 , GRCh37.p13 chr3: 131,097,978-131,098,061 NUDT16-DT
    nsv5555577mobile element insertion1nstd206human GRCh38 chr3: 131,350,935-131,350,986 , GRCh37.p13 chr3: 131,069,779-131,069,830 NEK11, NUDT16-DT
    nsv5451554copy number variation1nstd206human GRCh38 chr3: 131,271,919-131,477,783 , GRCh37.p13 chr3: 130,990,763-131,196,627 MRPL3, NEK11, 6 more genes
    nsv5449190copy number variation1nstd206human GRCh38 chr3: 131,351,000-131,408,000 , GRCh37.p13 chr3: 131,069,844-131,126,844 NUDT16-DT, NUDT16, 2 more genes
    nsv5448933copy number variation1nstd206human GRCh38 chr3: 131,379,137-131,379,218 , GRCh37.p13 chr3: 131,097,981-131,098,062 NUDT16-DT
    nsv5445729copy number variation1nstd206human GRCh38 chr3: 131,352,614-131,352,690 , GRCh37.p13 chr3: 131,071,458-131,071,534 NUDT16-DT
    nsv5443881copy number variation1nstd206human GRCh38 chr3: 131,350,127-131,350,225 , GRCh37.p13 chr3: 131,068,971-131,069,069 NUDT16-DT, NEK11
    nsv5442876copy number variation1nstd206human GRCh38 chr3: 131,358,877-131,358,932 , GRCh37.p13 chr3: 131,077,721-131,077,776 NUDT16-DT
    nsv5440291copy number variation1nstd206human GRCh38 chr3: 131,362,328-131,382,265 , GRCh37.p13 chr3: 131,081,172-131,101,109 NUDT16, NUDT16-DT, 1 more genes
    nsv5346534translocation1nstd200human GRCh38 chr3: 131,379,137-131,379,137 , GRCh38 chr3: 131,379,218-131,379,218 , GRCh37.p13 chr3: 131,097,981-131,097,981 , GRCh37.p13 chr3: 131,098,062-131,098,062 NUDT16-DT
    nsv5336557translocation1nstd200human GRCh37 chr3: 131,097,981-131,097,981 , GRCh37 chr3: 131,098,062-131,098,062 , GRCh38.p12 chr3: 131,379,137-131,379,137 , GRCh38.p12 chr3: 131,379,218-131,379,218 NUDT16-DT
    nsv5177487mobile element insertion1nstd203human GRCh38 chr3: 131,350,923-131,350,935 , GRCh37.p13 chr3: 131,069,767-131,069,779 NEK11, NUDT16-DT
    nsv5172635mobile element insertion1nstd203human GRCh38 chr3: 131,350,928-131,350,935 , GRCh37.p13 chr3: 131,069,772-131,069,779 NUDT16-DT, NEK11
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