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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095142copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 29,575,982-29,662,069 , GRCh38.p12 chr17: 31,248,964-31,335,051 EVI2A, EVI2B, 3 more genes
    nsv7095094copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,592,237-29,701,173 , GRCh38.p12 chr17: 31,265,219-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv7095093copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,575,982-29,665,843 , GRCh38.p12 chr17: 31,248,964-31,338,825 NF1, LOC101927057, 3 more genes
    nsv7095089copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,527,420-29,701,173 , GRCh38.p12 chr17: 31,200,402-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv7095088copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,422,328-29,677,356 , GRCh38.p12 chr17: 31,095,310-31,350,338 AK4P1, EVI2A, 4 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094967copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,559,879-29,685,283 , GRCh38.p12 chr17: 31,232,861-31,358,265 AK4P1, EVI2A, 4 more genes
    nsv7094876copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr17: 29,585,352-29,670,163 , GRCh38.p12 chr17: 31,258,334-31,343,145 EVI2A, EVI2B, 3 more genes
    nsv7094873copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,562,619-29,701,173 , GRCh38.p12 chr17: 31,235,601-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv7094872copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,556,833-29,701,173 , GRCh38.p12 chr17: 31,229,815-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv7094870copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,541,449-29,701,173 , GRCh38.p12 chr17: 31,214,431-31,374,155 AK4P1, EVI2A, 4 more genes
    nsv7094866copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,422,055-29,662,069 , GRCh38.p12 chr17: 31,095,037-31,335,051 EVI2A, EVI2B, 3 more genes
    nsv7063502inversion1nstd229human GRCh38 chr17: 30,624,449-32,040,578 , GRCh37.p13 chr17: 28,951,467-30,367,597 ATAD5, SH3GL1P2, 42 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6987354copy number variation1nstd229human GRCh38 chr17: 30,757,760-31,964,420 , GRCh37.p13 chr17: 29,084,778-30,291,439 EVI2A, OMG, 34 more genes
    nsv6983388copy number variation1nstd229human GRCh38 chr17: 31,215,740-31,333,469 , GRCh37.p13 chr17: 29,542,758-29,660,487 EVI2B, NF1, 3 more genes
    nsv6982533copy number variation1nstd229human GRCh38 chr17: 30,657,528-32,073,539 , GRCh37.p13 chr17: 28,984,546-30,400,558 UTP6, LOC107984974, 38 more genes
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6634407copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,076,232-30,043,725 , GRCh38.p12 chr17: 30,749,214-31,716,706 RAB11FIP4, RNU6-1134P, 29 more genes
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