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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130995insertion1nstd186human GRCh37 chr17: 36,090,006-36,090,008 , GRCh38.p12 chr17: 37,730,015-37,730,017 , GRCh38.p12 chr17|NT_187614.1: 1,969,071-1,969,073 HNF1B
    nsv6112791copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,815,466-36,249,366 , GRCh38.p12 chr17|NT_187614.1: 694,556-2,128,431 , GRCh38.p12 chr17: 36,459,652-37,889,744 HNF1B, LOC107985031, 36 more genes
    nsv5946301copy number variation1nstd209human GRCh38 chr17: 37,715,872-37,716,383 , GRCh37.p13 chr17: 36,075,880-36,076,391 HNF1B, LOC105371754
    nsv5932561copy number variation1nstd209human GRCh38 chr17: 36,271,341-37,995,711 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC101060212, RNU6-1192P, 47 more genes
    nsv5709752mobile element insertion2nstd211human GRCh38 chr17: 37,712,452-37,712,452 , GRCh37.p13 chr17: 36,072,460-36,072,460 HNF1B, LOC105371754
    nsv5697624mobile element insertion1nstd211human GRCh38 chr17: 37,736,407-37,736,407 , GRCh37.p13 chr17: 36,096,397-36,096,397 HNF1B
    nsv5662334insertion1nstd207human GRCh38 chr17: 37,712,436-37,712,436 , GRCh37.p13 chr17: 36,072,444-36,072,444 HNF1B, LOC105371754
    nsv5652825insertion1nstd207human GRCh38 chr17: 37,729,966-37,729,966 , GRCh37.p13 chr17: 36,089,957-36,089,957 HNF1B
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5552699insertion1nstd206human GRCh38 chr17: 37,730,015-37,730,017 , GRCh37.p13 chr17: 36,090,006-36,090,008 HNF1B
    nsv5516549copy number variation1nstd206human GRCh38 chr17: 37,715,852-37,716,405 , GRCh37.p13 chr17: 36,075,860-36,076,413 HNF1B, LOC105371754
    nsv5424583mobile element insertion1nstd206human GRCh38 chr17: 37,712,452-37,712,503 , GRCh37.p13 chr17: 36,072,460-36,072,511 LOC105371754, HNF1B
    nsv5420318mobile element insertion1nstd206human GRCh38 chr17: 37,736,407-37,736,458 , GRCh37.p13 chr17: 36,096,397-36,096,448 HNF1B
    nsv5293959copy number variation1nstd204human GRCh38.p13 chr17: 37,688,595-37,690,281 , GRCh37.p13 chr17: 36,048,600-36,050,286 LOC105371755, HNF1B
    nsv5200381copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,817,422-36,243,028 , GRCh38.p12 chr17: 36,461,608-37,883,408 , GRCh38.p12 chr17|NT_187614.1: 696,512-2,122,093 MRM1, LOC105379600, 36 more genes
    nsv5200379copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,437,475-36,243,028 , GRCh38.p12 chr17: 36,110,082-37,883,408 , GRCh38.p12 chr17|NT_187614.1: 345,003-2,122,093 DUSP14, RPS2P49, 54 more genes
    nsv5151484mobile element insertion1nstd203human GRCh38 chr17: 37,712,436-37,712,452 , GRCh37.p13 chr17: 36,072,444-36,072,460 LOC105371754, HNF1B
    nsv5142825mobile element insertion1nstd203human GRCh38 chr17: 37,713,468-37,713,482 , GRCh37.p13 chr17: 36,073,476-36,073,490 LOC105371754, HNF1B
    nsv5016212copy number variation1nstd200human GRCh38 chr17: 37,743,345-37,744,213 , GRCh37.p13 chr17: 36,103,336-36,104,204 HNF1B
    nsv5016211copy number variation1nstd200human GRCh38 chr17: 37,742,113-37,742,201 , GRCh37.p13 chr17: 36,102,104-36,102,192 HNF1B
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