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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941706copy number variation1nstd209human GRCh38 chr17: 41,082,720-41,103,904 , GRCh37.p13 chr17: 39,238,972-39,260,156 KRTAP4-16, KRTAP4-8, 2 more genes
    nsv5931375copy number variation1nstd209human GRCh38 chr17: 41,097,890-41,118,120 , GRCh37.p13 chr17: 39,254,142-39,274,372 KRTAP4-11, KRTAP4-16, 2 more genes
    nsv5886811copy number variation1nstd209human GRCh38 chr17: 41,104,822-41,109,172 , GRCh37.p13 chr17: 39,261,074-39,265,424 KRTAP4-9
    nsv5877483copy number variation1nstd209human GRCh38 chr17: 41,105,373-41,123,175 , GRCh37.p13 chr17: 39,261,625-39,279,427 KRTAP4-9, KRTAP4-12, 1 more genes
    nsv5874279copy number variation2nstd209human GRCh38 chr17: 41,100,090-41,104,528 , GRCh37.p13 chr17: 39,256,342-39,260,780 KRTAP4-16, KRTAP4-9
    nsv5873067copy number variation2nstd209human GRCh38 chr17: 41,103,029-41,104,410 , GRCh37.p13 chr17: 39,259,281-39,260,662 KRTAP4-9
    nsv5591863copy number variation1nstd207human GRCh38 chr17: 41,105,490-41,105,609 , GRCh37.p13 chr17: 39,261,742-39,261,861 KRTAP4-9
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5524517copy number variation1nstd206human GRCh38 chr17: 41,099,350-41,119,980 , GRCh37.p13 chr17: 39,255,602-39,276,232 KRTAP4-11, KRTAP4-16, 1 more genes
    nsv5523699copy number variation1nstd206human GRCh38 chr17: 41,083,980-41,105,980 , GRCh37.p13 chr17: 39,240,232-39,262,232 KRTAP4-16, KRTAP4-8, 2 more genes
    nsv5518631copy number variation1nstd206human GRCh38 chr17: 40,902,081-41,114,453 , GRCh37.p13 chr17: 39,058,333-39,270,705 KRTAP2-3, LOC105371777, 20 more genes
    nsv5517814copy number variation1nstd206human GRCh38 chr17: 41,089,000-41,108,100 , GRCh37.p13 chr17: 39,245,252-39,264,352 KRTAP4-8, KRTAP4-9, 1 more genes
    nsv5324997copy number variation1nstd204human GRCh37.p13 chr17: 39,208,885-39,260,697 , GRCh38.p13 chr17: 41,052,633-41,104,445 KRTAP2-4, KRTAP2-5P, 6 more genes
    nsv5292123copy number variation1nstd204human GRCh38.p13 chr17: 41,083,808-41,103,710 , GRCh37.p13 chr17: 39,240,060-39,259,962 KRTAP4-8, KRTAP4-16, 2 more genes
    nsv5016362copy number variation1nstd200human GRCh38 chr17: 41,099,951-41,120,531 , GRCh37.p13 chr17: 39,256,203-39,276,783 KRTAP4-16, KRTAP4-9, 1 more genes
    nsv5016360copy number variation1nstd200human GRCh38 chr17: 41,093,416-41,113,979 , GRCh37.p13 chr17: 39,249,668-39,270,231 KRTAP4-8, KRTAP4-9, 1 more genes
    nsv5013697copy number variation1nstd200human GRCh38 chr17: 41,093,093-41,113,618 , GRCh37.p13 chr17: 39,249,345-39,269,870 KRTAP4-8, KRTAP4-9, 1 more genes
    nsv4864652copy number variation1nstd200human GRCh37 chr17: 39,208,915-39,260,675 , GRCh38.p12 chr17: 41,052,663-41,104,423 , GRCh38.p12 chr17|NW_003871091.1: 202,056-254,110 KRTAP2-3, KRTAP2-5P, 7 more genes
    nsv4858808copy number variation1nstd200human GRCh37 chr17: 39,256,763-39,276,978 , GRCh38.p12 chr17|NW_003871091.1: 250,198-270,477 , GRCh38.p12 chr17: 41,100,511-41,120,726 KRTAP4-11, KRTAP4-9, 1 more genes
    nsv4858806copy number variation1nstd200human GRCh37 chr17: 39,249,688-39,270,067 , GRCh38.p12 chr17|NW_003871091.1: 243,094-263,565 , GRCh38.p12 chr17: 41,093,436-41,113,815 KRTAP4-16, KRTAP4-9, 1 more genes
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