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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5701410mobile element insertion1nstd211human GRCh38 chr17: 51,157,577-51,157,577 , GRCh37.p13 chr17: 49,234,938-49,234,938 NME1, NME1-NME2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5553539insertion1nstd206human GRCh38 chr17: 51,157,527-51,157,577 , GRCh37.p13 chr17: 49,234,888-49,234,938 NME1, NME1-NME2
    nsv5520921copy number variation1nstd206human GRCh38 chr17: 51,150,447-51,157,577 , GRCh37.p13 chr17: 49,227,808-49,234,938 NME1, NME1-NME2
    nsv5517298copy number variation1nstd206human GRCh38 chr17: 51,148,587-51,152,102 , GRCh37.p13 chr17: 49,225,948-49,229,463 NME1, NME1-NME2
    nsv5358939translocation1nstd200human GRCh38 chr17: 51,151,993-51,151,993 , GRCh38 chr17: 51,152,071-51,152,071 , GRCh37.p13 chr17: 49,229,354-49,229,354 , GRCh37.p13 chr17: 49,229,432-49,229,432 NME1-NME2, NME1
    nsv5320658copy number variation1nstd204human GRCh37.p13 chr17: 49,245,074-49,255,945 , GRCh38.p13 chr17: 51,167,713-51,178,584 NME2, MBTD1, 1 more genes
    nsv5026413copy number variation1nstd200human GRCh38 chr17: 51,150,664-51,157,606 , GRCh37.p13 chr17: 49,228,025-49,234,967 NME1, NME1-NME2
    nsv5026412copy number variation1nstd200human GRCh38 chr17: 51,150,227-51,152,316 , GRCh37.p13 chr17: 49,227,588-49,229,677 NME1, NME1-NME2
    nsv4867277copy number variation1nstd200human GRCh37 chr17: 49,228,053-49,234,938 , GRCh38.p12 chr17: 51,150,692-51,157,577 NME1-NME2, NME1
    nsv4575215mobile element insertion1nstd166human GRCh37.p13 chr17: 49,241,024-49,241,024 , GRCh38.p12 chr17: 51,163,663-51,163,663 NME1-NME2, NME2
    nsv4531356copy number variation1nstd166human GRCh37.p13 chr17: 49,230,921-49,231,520 , GRCh38.p12 chr17: 51,153,560-51,154,159 NME1-NME2, NME1
    nsv4512329mobile element insertion1nstd166human GRCh37.p13 chr17: 49,248,874-49,248,874 , GRCh38.p12 chr17: 51,171,513-51,171,513 NME2, NME1-NME2
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4261711copy number variation1nstd166human GRCh37.p13 chr17: 49,228,142-49,234,938 , GRCh38.p12 chr17: 51,150,781-51,157,577 NME1, NME1-NME2
    nsv4257844copy number variation1nstd166human GRCh37.p13 chr17: 49,229,450-49,229,510 , GRCh38.p12 chr17: 51,152,089-51,152,149 NME1, NME1-NME2
    nsv4256592copy number variation1nstd166human GRCh37.p13 chr17: 49,079,290-49,237,725 , GRCh38.p12 chr17: 51,001,929-51,160,364 NME1, NME1-NME2, 1 more genes
    nsv4255505copy number variation1nstd166human GRCh37.p13 chr17: 49,246,133-49,246,579 , GRCh38.p12 chr17: 51,168,772-51,169,218 NME1-NME2, NME2
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
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