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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124019copy number variation1nstd186human GRCh37 chr17: 39,197,506-39,197,593 , GRCh38.p12 chr17: 41,041,254-41,041,341 , GRCh38.p12 chr17|NW_003871091.1: 190,647-190,734 KRTAP1-1
    nsv5942887copy number variation1nstd209human GRCh38 chr17: 41,038,106-41,039,531 , GRCh37.p13 chr17: 39,194,358-39,195,783 KRTAP1-1
    nsv5933786copy number variation1nstd209human GRCh38 chr17: 41,041,248-41,041,385 , GRCh37.p13 chr17: 39,197,500-39,197,637 KRTAP1-1
    nsv5930057copy number variation1nstd209human GRCh38 chr17: 41,034,751-41,041,296 , GRCh37.p13 chr17: 39,191,003-39,197,548 KRTAP1-1, KRTAP1-3
    nsv5590808copy number variation1nstd207human GRCh38 chr17: 41,041,248-41,041,385 , GRCh37.p13 chr17: 39,197,500-39,197,637 KRTAP1-1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5527780copy number variation1nstd206human GRCh38 chr17: 41,033,482-41,038,961 , GRCh37.p13 chr17: 39,189,734-39,195,213 KRTAP1-3, KRTAP1-1
    nsv5527307copy number variation1nstd206human GRCh38 chr17: 41,038,086-41,039,552 , GRCh37.p13 chr17: 39,194,338-39,195,804 KRTAP1-1
    nsv5521681copy number variation1nstd206human GRCh38 chr17: 41,041,254-41,041,341 , GRCh37.p13 chr17: 39,197,506-39,197,593 KRTAP1-1
    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
    nsv5016356copy number variation1nstd200human GRCh38 chr17: 41,040,440-41,049,879 , GRCh37.p13 chr17: 39,196,692-39,206,131 KRTAP2-1, KRTAP1-1
    nsv5016355copy number variation1nstd200human GRCh38 chr17: 41,033,482-41,038,961 , GRCh37.p13 chr17: 39,189,734-39,195,213 KRTAP1-3, KRTAP1-1
    nsv4864651copy number variation1nstd200human GRCh37 chr17: 39,194,358-39,195,784 , GRCh38.p12 chr17: 41,038,106-41,039,532 , GRCh38.p12 chr17|NW_003871091.1: 187,499-188,925 KRTAP1-1
    nsv4858803copy number variation1nstd200human GRCh37 chr17: 39,196,670-39,206,140 , GRCh38.p12 chr17|NW_003871091.1: 189,811-199,281 , GRCh38.p12 chr17: 41,040,418-41,049,888 KRTAP2-1, KRTAP1-1
    nsv4858802copy number variation1nstd200human GRCh37 chr17: 39,189,734-39,195,213 , GRCh38.p12 chr17|NW_003871091.1: 182,877-188,354 , GRCh38.p12 chr17: 41,033,482-41,038,961 KRTAP1-3, KRTAP1-1
    nsv4742568copy number variation1nstd199human GRCh37 chr17: 39,197,459-39,197,599 , GRCh38.p12 chr17|NW_003871091.1: 190,600-190,740 , GRCh38.p12 chr17: 41,041,207-41,041,347 KRTAP1-1
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 more genes
    nsv4437875copy number variation1nstd175human GRCh37 chr17: 39,197,500-39,197,638 , GRCh38.p12 chr17: 41,041,248-41,041,386 , GRCh38.p12 chr17|NW_003871091.1: 190,641-190,779 KRTAP1-1
    nsv4426409copy number variation1nstd174human GRCh37 chr17: 39,191,188-39,222,806 , GRCh38.p12 chr17: 41,034,936-41,066,554 , GRCh38.p12 chr17|NW_003871091.1: 184,331-216,052 KRTAP1-3, KRTAP1-1, 4 more genes
    nsv4422744copy number variation1nstd174human GRCh37 chr17: 39,196,933-39,198,466 , GRCh38.p12 chr17|NW_003871091.1: 190,074-191,607 , GRCh38.p12 chr17: 41,040,681-41,042,214 KRTAP1-1
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