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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995523copy number variation1nstd229human GRCh38 chr17: 52,365,430-53,670,410 , GRCh37.p13 chr17: 50,442,790-51,747,771 LOC645163, LINC02089, 5 more genes
    nsv6992502copy number variation1nstd229human GRCh38 chr17: 52,187,301-54,706,500 , GRCh37.p13 chr17: 50,264,661-52,783,861 RPS2P48, LOC107985001, 12 more genes
    nsv6989550copy number variation1nstd229human GRCh38 chr17: 52,873,916-53,237,272 , GRCh37.p13 chr17: 50,951,276-51,314,633 LINC02089, LINC02876, 2 more genes
    nsv6987204copy number variation1nstd229human GRCh38 chr17: 52,915,895-53,052,228 , GRCh37.p13 chr17: 50,993,255-51,129,589 LOC107984983, LINC02876
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6985275copy number variation1nstd229human GRCh38 chr17: 51,947,077-54,771,149 , GRCh37.p13 chr17: 50,024,437-52,848,510 LOC100128713, LOC645163, 15 more genes
    nsv6984292copy number variation1nstd229human GRCh38 chr17: 52,986,465-53,683,051 , GRCh37.p13 chr17: 51,063,825-51,760,412 LOC645163, MTCO1P40, 2 more genes
    nsv6981408copy number variation1nstd229human GRCh38 chr17: 52,873,861-53,022,121 , GRCh37.p13 chr17: 50,951,221-51,099,481 LINC02089, LOC107984983, 1 more genes
    nsv6635744copy number variation1nstd227human GRCh37 chr17: 50,995,495-51,129,039 , GRCh38.p12 chr17: 52,918,135-53,051,678 LINC02876, LOC107984983
    nsv6635146copy number variation2nstd227human GRCh37 chr17: 50,949,615-51,314,354 , GRCh38.p12 chr17: 52,872,255-53,236,993 LINC02876, LINC02089, 2 more genes
    nsv6624254copy number variation4nstd224human GRCh37 chr17: 50,963,927-51,313,965 , GRCh38.p12 chr17: 52,886,567-53,236,604 LINC02089, MTCO1P40, 2 more genes
    nsv6587456inversion1nstd223human GRCh38 chr17: 52,409,512-53,222,775 , GRCh37.p13 chr17: 50,486,872-51,300,136 LINC02876, LINC01982, 3 more genes
    nsv6525250copy number variation1nstd223human GRCh38 chr17: 52,873,915-53,022,120 , GRCh37.p13 chr17: 50,951,275-51,099,480 LINC02876, LINC02089, 1 more genes
    nsv6520863copy number variation1nstd223human GRCh38 chr17: 52,873,914-53,237,270 , GRCh37.p13 chr17: 50,951,274-51,314,631 MTCO1P40, LOC107984983, 2 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
    nsv5528796copy number variation1nstd206human GRCh38 chr17: 52,958,440-52,992,288 , GRCh37.p13 chr17: 51,035,800-51,069,648 LINC02876
    nsv5517967copy number variation1nstd206human GRCh38 chr17: 52,982,892-52,988,292 , GRCh37.p13 chr17: 51,060,252-51,065,652 LINC02876
    nsv5374956translocation1nstd200human GRCh38 chr17: 52,985,177-52,985,177 , GRCh38 chr17: 52,984,476-52,984,476 , GRCh37.p13 chr17: 51,061,836-51,061,836 , GRCh37.p13 chr17: 51,062,537-51,062,537 LINC02876
    nsv5374955translocation1nstd200human GRCh38 chr17: 52,985,353-52,985,353 , GRCh38 chr17: 52,984,470-52,984,470 , GRCh37.p13 chr17: 51,061,830-51,061,830 , GRCh37.p13 chr17: 51,062,713-51,062,713 LINC02876
    nsv5343884translocation1nstd200human GRCh37 chr17: 51,061,830-51,061,830 , GRCh37 chr17: 51,062,713-51,062,713 , GRCh38.p12 chr17: 52,984,470-52,984,470 , GRCh38.p12 chr17: 52,985,353-52,985,353 LINC02876
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