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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937790copy number variation1nstd209human GRCh38 chr17: 30,668,045-32,084,125 , GRCh37.p13 chr17: 28,995,063-30,411,144 , OMG, 39 more genes
    nsv5561493sequence alteration1nstd206human GRCh37.p13 chr17: 30,380,978-30,536,565 , GRCh38 chr17: 32,053,959-32,209,546 RHOT1, LRRC37B, 4 more genes
    nsv5559407mobile element insertion1nstd206human GRCh38 chr17: 32,008,593-32,008,593 , GRCh37.p13 chr17: 30,335,612-30,335,612 LRRC37B
    nsv5517367copy number variation1nstd206human GRCh38 chr17: 32,053,980-32,064,000 , GRCh37.p13 chr17: 30,380,999-30,391,019 LRRC37B
    nsv5374893translocation1nstd200human GRCh38 chr17: 32,012,023-32,012,023 , GRCh38 chr17: 32,008,594-32,008,594 , GRCh37.p13 chr17: 30,339,042-30,339,042 , GRCh37.p13 chr17: 30,335,613-30,335,613 LRRC37B
    nsv5374892translocation1nstd200human GRCh38 chr17: 32,008,594-32,008,594 , GRCh38 chr17: 32,011,779-32,011,779 , GRCh37.p13 chr17: 30,338,798-30,338,798 , GRCh37.p13 chr17: 30,335,613-30,335,613 LRRC37B
    nsv5365762translocation1nstd200human GRCh38 chrX: 83,952,356-83,952,356 , GRCh38 chr17: 32,051,564-32,051,564 , GRCh37.p13 chrX: 83,207,364-83,207,364 , GRCh37.p13 chr17: 30,378,583-30,378,583 LRRC37B
    nsv5365761translocation1nstd200human GRCh38 chrX: 83,952,754-83,952,754 , GRCh38 chr17: 32,051,041-32,051,041 , GRCh37.p13 chrX: 83,207,762-83,207,762 , GRCh37.p13 chr17: 30,378,060-30,378,060 LRRC37B
    nsv5299964copy number variation1nstd204human GRCh38.p13 chr17: 32,050,487-32,051,829 , GRCh37.p13 chr17: 30,377,506-30,378,848 LRRC37B
    nsv5298444copy number variation1nstd204human GRCh38.p13 chr17: 31,949,801-32,025,000 , GRCh37.p13 chr17: 30,276,820-30,352,019 SUZ12, LRRC37B, 1 more genes
    nsv5285756copy number variation1nstd204human GRCh38.p13 chr17: 32,046,753-32,062,289 , GRCh37.p13 chr17: 30,373,772-30,389,308 , LRRC37B
    nsv5158619mobile element insertion1nstd203human GRCh38 chr17: 32,038,416-32,038,449 , GRCh37.p13 chr17: 30,365,435-30,365,468 SH3GL1P1, LRRC37B
    nsv5016034copy number variation1nstd200human GRCh38 chr17: 32,039,420-32,044,805 , GRCh37.p13 chr17: 30,366,439-30,371,824 LRRC37B, SH3GL1P1
    nsv4858590copy number variation1nstd200human GRCh37 chr17: 30,366,439-30,371,824 , GRCh38.p12 chr17: 32,039,420-32,044,805 SH3GL1P1, LRRC37B
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729951copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,989,741-32,355,632 , GRCh38.p12 chr17: 31,662,722-34,028,613 RNA5SP437, PSMD11, 34 more genes
    nsv4729791copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769 ADAP2, TEFM, 37 more genes
    nsv4708434copy number variation1nstd195human GRCh37 chr17: 30,372,701-30,373,651 , GRCh38.p12 chr17: 32,045,682-32,046,632 , LRRC37B
    nsv4684241copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,393,104-30,427,403 , GRCh38.p12 chr17: 31,066,086-32,100,384 LOC102724625, RNA5SP437, 26 more genes
    nsv4675844copy number variation1nstd102humanUncertain significance GRCh37 chr17: 30,306,459-30,537,745 , GRCh38.p12 chr17: 31,979,440-32,210,726 LOC105371730, LRRC37B, 6 more genes
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