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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137156copy number variation1nstd233human GRCh37.p13 chr17: 59,529,098-60,599,347 , GRCh38 chr17: 61,451,737-62,521,986 TBX4, MED13, 20 more genes
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7070223inversion1nstd229human GRCh38 chr17: 61,482,736-62,369,304 , GRCh37.p13 chr17: 59,560,097-60,446,665 TBC1D3P2, TBX4, 12 more genes
    nsv6637728copy number variation1nstd102humanUncertain significance GRCh37 chr17: 60,070,415-60,450,079 , GRCh38.p12 chr17: 61,993,054-62,372,718 MED13, LOC100996361, 8 more genes
    nsv6624498copy number variation1nstd224human GRCh37 chr17: 60,199,130-60,440,732 , GRCh38.p12 chr17: 62,121,769-62,363,371 POLRMTP1, TBC1D3P2, 5 more genes
    nsv6531321copy number variation1nstd223human GRCh38 chr17: 61,981,221-62,425,637 , GRCh37.p13 chr17: 60,058,582-60,502,998 TBC1D3P2, RPL36AP47, 13 more genes
    nsv6289794copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,076,721-60,362,868 , GRCh38.p12 chr17: 59,999,360-62,285,507 CA4, TBX2, 49 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5327819copy number variation1nstd204human GRCh37.p13 chr17: 60,346,903-60,356,966 , GRCh38.p13 chr17: 62,269,542-62,279,605 TBC1D3P2, LOC105371853
    nsv5300165copy number variation1nstd204human GRCh38.p13 chr17: 62,269,601-62,279,500 , GRCh37.p13 chr17: 60,346,962-60,356,861 LOC105371853, TBC1D3P2
    nsv5297570copy number variation1nstd204human GRCh38.p13 chr17: 62,269,478-62,279,496 , GRCh37.p13 chr17: 60,346,839-60,356,857 TBC1D3P2, LOC105371853
    nsv5281660copy number variation1nstd204human GRCh38.p13 chr17: 62,246,258-62,262,918 , GRCh37.p13 chr17: 60,323,619-60,340,279 TBC1D3P2, LOC100996361
    nsv5013898copy number variation1nstd200human GRCh38 chr17: 62,225,835-62,280,888 , GRCh37.p13 chr17: 60,303,196-60,358,249 LOC100996361, LOC105371853, 2 more genes
    nsv5013891copy number variation1nstd200human GRCh38 chr17: 62,115,455-62,351,528 , GRCh37.p13 chr17: 60,192,816-60,428,889 RPL36AP47, POLRMTP1, 5 more genes
    nsv5013890copy number variation1nstd200human GRCh38 chr17: 61,981,265-62,425,676 , GRCh37.p13 chr17: 60,058,626-60,503,037 TBC1D3P2, LOC105371853, 13 more genes
    nsv5010536copy number variation1nstd200human GRCh38 chr17: 62,269,567-62,279,577 , GRCh37.p13 chr17: 60,346,928-60,356,938 TBC1D3P2, LOC105371853
    nsv4851593copy number variation1nstd200human GRCh37 chr17: 60,346,928-60,356,937 , GRCh38.p12 chr17: 62,269,567-62,279,576 TBC1D3P2, LOC105371853
    nsv4670647copy number variation1nstd186human GRCh37 chr17: 60,342,014-60,345,441 , GRCh38.p12 chr17: 62,264,653-62,268,080 TBC1D3P2
    nsv4670423copy number variation1nstd186human GRCh37 chr17: 60,344,590-60,345,542 , GRCh38.p12 chr17: 62,267,229-62,268,181 TBC1D3P2
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