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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118995copy number variation1nstd186human GRCh37 chr1: 158,959,869-158,959,932 , GRCh38.p12 chr1: 158,990,079-158,990,142 PYHIN1
    nsv5963265insertion1nstd209human GRCh38 chr1: 158,968,820-158,968,820 , GRCh37.p13 chr1: 158,938,610-158,938,610 PYHIN1
    nsv5720061mobile element insertion2nstd211human GRCh38 chr1: 158,939,951-158,939,951 , GRCh37.p13 chr1: 158,909,741-158,909,741 PYHIN1
    nsv5611911insertion1nstd207human GRCh38 chr1: 158,990,078-158,990,078 , GRCh37.p13 chr1: 158,959,868-158,959,868 PYHIN1
    nsv5554248mobile element insertion1nstd206human GRCh38 chr1: 158,939,951-158,940,002 , GRCh37.p13 chr1: 158,909,741-158,909,792 PYHIN1
    nsv5433515copy number variation1nstd206human GRCh38 chr1: 158,932,938-158,933,115 , GRCh37.p13 chr1: 158,902,728-158,902,905 PYHIN1
    nsv5427914copy number variation1nstd206human GRCh38 chr1: 158,939,312-158,939,369 , GRCh37.p13 chr1: 158,909,102-158,909,159 PYHIN1
    nsv5426745copy number variation1nstd206human GRCh38 chr1: 158,990,079-158,990,142 , GRCh37.p13 chr1: 158,959,869-158,959,932 PYHIN1
    nsv5420186copy number variation1nstd206human GRCh38 chr1: 158,890,587-158,956,587 , GRCh37.p13 chr1: 158,860,377-158,926,377 PYHIN1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5361483translocation1nstd200human GRCh38 chr1: 158,933,115-158,933,115 , GRCh38 chr1: 158,932,938-158,932,938 , GRCh37.p13 chr1: 158,902,728-158,902,728 , GRCh37.p13 chr1: 158,902,905-158,902,905 PYHIN1
    nsv5297301copy number variation1nstd204human GRCh38.p13 chr1: 158,960,846-158,975,515 , GRCh37.p13 chr1: 158,930,636-158,945,305 PYHIN1
    nsv5217952copy number variation1nstd204human GRCh38.p13 chr1: 158,962,483-158,963,782 , GRCh37.p13 chr1: 158,932,273-158,933,572 PYHIN1
    nsv5216721copy number variation1nstd204human GRCh38.p13 chr1: 158,988,401-158,996,400 , GRCh37.p13 chr1: 158,958,191-158,966,190 PYHIN1
    nsv5210047copy number variation1nstd204human GRCh38.p13 chr1: 158,989,501-158,997,900 , GRCh37.p13 chr1: 158,959,291-158,967,690 PYHIN1
    nsv5207963copy number variation1nstd204human GRCh38.p13 chr1: 158,983,337-158,984,336 , GRCh37.p13 chr1: 158,953,127-158,954,126 PYHIN1
    nsv5205260copy number variation1nstd204human GRCh38.p13 chr1: 158,960,383-158,968,782 , GRCh37.p13 chr1: 158,930,173-158,938,572 PYHIN1
    nsv5071455mobile element insertion1nstd203human GRCh38 chr1: 158,988,351-158,988,363 , GRCh37.p13 chr1: 158,958,141-158,958,153 PYHIN1
    nsv5061245mobile element insertion1nstd203human GRCh38 chr1: 158,964,719-158,964,735 , GRCh37.p13 chr1: 158,934,509-158,934,525 PYHIN1
    nsv4784405copy number variation1nstd200human GRCh37 chr1: 158,902,728-158,902,905 , GRCh38.p12 chr1: 158,932,938-158,933,115 PYHIN1
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