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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940503copy number variation1nstd209human GRCh38 chr17: 43,181,868-43,183,532 , GRCh37.p13 chr17: 41,333,885-41,335,549 NBR1
    nsv5879002copy number variation1nstd209human GRCh38 chr17: 43,181,841-43,183,590 , GRCh37.p13 chr17: 41,333,858-41,335,607 NBR1
    nsv5873068copy number variation1nstd209human GRCh38 chr17: 43,175,502-43,176,501 , GRCh37.p13 chr17: 41,327,519-41,328,518 NBR1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5532670copy number variation1nstd206human GRCh38 chr17: 43,190,257-43,207,008 , GRCh37.p13 chr17: 41,342,274-41,359,027 NBR1
    nsv5526735copy number variation1nstd206human GRCh38 chr17: 43,193,811-43,193,892 , GRCh37.p13 chr17: 41,345,828-41,345,909 NBR1
    nsv5520425copy number variation1nstd206human GRCh38 chr17: 43,181,868-43,183,533 , GRCh37.p13 chr17: 41,333,885-41,335,550 NBR1
    nsv5514323copy number variation1nstd206human GRCh38 chr17: 43,102,678-43,183,624 , GRCh37.p13 chr17: 41,254,695-41,335,641 BRCA1, NBR1, 4 more genes
    nsv5322827copy number variation1nstd204human GRCh38.p13 chr17: 43,181,842-43,183,558 , GRCh37.p13 chr17: 41,333,859-41,335,575 NBR1
    nsv5292303copy number variation1nstd204human GRCh38.p13 chr17: 43,185,191-43,194,160 , GRCh37.p13 chr17: 41,337,208-41,346,177 NBR1
    nsv5292045copy number variation1nstd204human GRCh38.p13 chr17: 43,182,091-43,183,690 , GRCh37.p13 chr17: 41,334,108-41,335,707 NBR1
    nsv5291965copy number variation1nstd204human GRCh38.p13 chr17: 43,161,304-43,170,001 , GRCh37.p13 chr17: 41,313,321-41,322,018 LOC101929767, NBR1, 1 more genes
    nsv5289818copy number variation1nstd204human GRCh38.p13 chr17: 43,159,701-43,231,500 , GRCh37.p13 chr17: 41,311,718-41,383,489 CCDC200, LOC101929767, 3 more genes
    nsv5288617copy number variation1nstd204human GRCh38.p13 chr17: 43,204,704-43,215,136 , GRCh37.p13 chr17: 41,356,721-41,367,155 TMEM106A, NBR1
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
    nsv5285495copy number variation1nstd204human GRCh38.p13 chr17: 43,191,018-43,201,703 , GRCh37.p13 chr17: 41,343,035-41,353,720 NBR1
    nsv5280768copy number variation1nstd204human GRCh38.p13 chr17: 43,171,927-43,179,440 , GRCh37.p13 chr17: 41,323,944-41,331,457 NBR1
    nsv5200272copy number variation1nstd205human GRCh37.p13 chr17: 41,242,185-41,378,464 , GRCh38.p12 chr17: 43,090,168-43,226,417 BRCA1, NBR1, 6 more genes
    nsv5140213mobile element insertion1nstd203human GRCh38 chr17: 43,204,715-43,204,733 , GRCh37.p13 chr17: 41,356,732-41,356,750 NBR1
    nsv5016471copy number variation1nstd200human GRCh38 chr17: 43,181,868-43,183,533 , GRCh37.p13 chr17: 41,333,885-41,335,550 NBR1
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