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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939766copy number variation1nstd209human GRCh38 chr17: 50,678,342-50,681,166 , GRCh37.p13 chr17: 48,755,703-48,758,527 ABCC3
    nsv5885027copy number variation2nstd209human GRCh38 chr17: 50,678,418-50,679,618 , GRCh37.p13 chr17: 48,755,779-48,756,979 ABCC3
    nsv5882800copy number variation1nstd209human GRCh38 chr17: 50,648,383-50,655,126 , GRCh37.p13 chr17: 48,725,744-48,732,487 ABCC3
    nsv5655043insertion1nstd207human GRCh38 chr17: 50,673,978-50,673,978 , GRCh37.p13 chr17: 48,751,339-48,751,339 ABCC3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530875copy number variation1nstd206human GRCh38 chr17: 50,660,866-50,661,025 , GRCh37.p13 chr17: 48,738,227-48,738,386 ABCC3
    nsv5527023copy number variation1nstd206human GRCh38 chr17: 50,666,884-50,666,945 , GRCh37.p13 chr17: 48,744,245-48,744,306 ABCC3
    nsv5026390copy number variation1nstd200human GRCh38 chr17: 50,683,020-50,685,985 , GRCh37.p13 chr17: 48,760,381-48,763,346 ABCC3
    nsv5026389copy number variation1nstd200human GRCh38 chr17: 50,673,666-50,679,136 , GRCh37.p13 chr17: 48,751,027-48,756,497 ABCC3
    nsv5026388copy number variation1nstd200human GRCh38 chr17: 50,656,722-50,660,096 , GRCh37.p13 chr17: 48,734,083-48,737,457 ABCC3
    nsv4867261copy number variation1nstd200human GRCh37 chr17: 48,760,381-48,763,346 , GRCh38.p12 chr17: 50,683,020-50,685,985 ABCC3
    nsv4740084copy number variation1nstd199human GRCh37 chr17: 48,751,299-48,751,391 , GRCh38.p12 chr17: 50,673,938-50,674,030 ABCC3
    nsv4557032insertion1nstd166human GRCh37.p13 chr17: 48,751,299-48,751,299 , GRCh38.p12 chr17: 50,673,938-50,673,938 ABCC3
    nsv4556505insertion1nstd166human GRCh37.p13 chr17: 48,751,281-48,751,281 , GRCh38.p12 chr17: 50,673,920-50,673,920 ABCC3
    nsv4532652copy number variation1nstd166human GRCh37.p13 chr17: 48,734,363-48,734,653 , GRCh38.p12 chr17: 50,657,002-50,657,292 ABCC3
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4255091copy number variation1nstd166human GRCh37.p13 chr17: 48,729,571-48,735,705 , GRCh38.p12 chr17: 50,652,210-50,658,344 ABCC3
    nsv4255008copy number variation1nstd166human GRCh37.p13 chr17: 48,719,145-48,721,786 , GRCh38.p12 chr17: 50,641,784-50,644,425 ABCC3
    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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