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Items: 1 to 20 of 663

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131623insertion1nstd186human GRCh37 chr17: 39,130,977-39,131,010 , GRCh38.p12 chr17|NW_003871091.1: 124,120-124,153 , GRCh38.p12 chr17: 40,974,725-40,974,758 LOC107985072
    nsv6130373insertion1nstd186human GRCh37 chr17: 39,130,743-39,130,771 , GRCh38.p12 chr17|NW_003871091.1: 123,886-123,914 , GRCh38.p12 chr17: 40,974,491-40,974,519 LOC107985072
    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
    nsv6123458copy number variation1nstd186human GRCh37 chr17: 39,203,202-39,211,742 , GRCh38.p12 chr17: 41,046,950-41,055,490 , GRCh38.p12 chr17|NW_003871091.1: 196,343-204,988 KRTAP2-2, KRTAP2-1
    nsv6116621mobile element insertion1nstd186human GRCh37 chr17: 39,177,031-39,177,082 , GRCh38.p12 chr17: 41,020,779-41,020,830 , GRCh38.p12 chr17|NW_003871091.1: 170,174-170,225 0
    nsv4864653copy number variation1nstd200human GRCh37 chr17: 39,274,259-39,280,302 , GRCh38.p12 chr17|NW_003871091.1: 267,757-273,786 , GRCh38.p12 chr17: 41,118,007-41,124,050 KRTAP4-12, KRTAP4-11
    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
    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
    nsv4864650copy number variation1nstd200human GRCh37 chr17: 39,036,012-39,036,477 , GRCh38.p12 chr17|NW_003871091.1: 29,028-29,493 , GRCh38.p12 chr17: 40,879,760-40,880,225 KRT20, LOC105371777
    nsv4858810copy number variation1nstd200human GRCh37 chr17: 39,274,478-39,280,275 , GRCh38.p12 chr17: 41,118,226-41,124,023 , GRCh38.p12 chr17|NW_003871091.1: 267,976-273,759 KRTAP4-12, KRTAP4-11
    nsv4858809copy number variation1nstd200human GRCh37 chr17: 39,265,875-39,289,132 , GRCh38.p12 chr17|NW_003871091.1: 259,345-278,132 , GRCh38.p12 chr17: 41,109,623-41,132,880 KRTAP4-12, KRTAP4-11
    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
    nsv4858807copy number variation1nstd200human GRCh37 chr17: 39,253,941-39,258,317 , GRCh38.p12 chr17: 41,097,689-41,102,065 , GRCh38.p12 chr17|NW_003871091.1: 247,347-251,752 KRTAP4-16, KRTAP4-8
    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
    nsv4858805copy number variation1nstd200human GRCh37 chr17: 39,247,659-39,248,632 , GRCh38.p12 chr17|NW_003871091.1: 241,065-242,038 , GRCh38.p12 chr17: 41,091,407-41,092,380 0
    nsv4858804copy number variation1nstd200human GRCh37 chr17: 39,228,116-39,228,181 , GRCh38.p12 chr17: 41,071,864-41,071,929 , GRCh38.p12 chr17|NW_003871091.1: 221,364-221,429 KRTAP2-5P
    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
    nsv4858801copy number variation1nstd200human GRCh37 chr17: 39,066,768-39,076,480 , GRCh38.p12 chr17: 40,910,516-40,920,228 , GRCh38.p12 chr17|NW_003871091.1: 59,784-69,496 LOC105371777
    nsv4858800copy number variation1nstd200human GRCh37 chr17: 39,065,969-39,135,860 , GRCh38.p12 chr17|NW_003871091.1: 58,985-129,003 , GRCh38.p12 chr17: 40,909,717-40,979,608 KRT23, KRT39, 3 more genes
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