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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7077200inversion1nstd229human GRCh38 chr17: 8,311,394-8,420,761 , GRCh37.p13 chr17: 8,214,712-8,324,079 LOC100128288, ARHGEF15, 4 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    nsv6499487copy number variation1nstd223human GRCh38 chr17: 8,390,066-8,397,372 , GRCh37.p13 chr17: 8,293,384-8,300,690 RNF222
    nsv6133428copy number variation1nstd213human GRCh37 chr17: 8,290,000-8,360,001 , GRCh38.p12 chr17: 8,386,682-8,456,683 NDEL1, RNF222
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv6026275copy number variation1nstd212human GRCh38 chr17: 8,388,795-8,388,857 , GRCh37.p13 chr17: 8,292,113-8,292,175 RNF222
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5281077copy number variation1nstd204human GRCh38.p13 chr17: 8,398,030-8,399,029 , GRCh37.p13 chr17: 8,301,348-8,302,347 RNF222
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4457674copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,676,383-8,350,870 , GRCh38.p12 chr17: 7,773,065-8,447,552 ARHGEF15, TRI-AAT4-1, 57 more genes
    nsv4240823copy number variation1nstd166human GRCh37.p13 chr17: 8,296,359-8,296,443 , GRCh38.p12 chr17: 8,393,041-8,393,125 RNF222
    nsv4232687copy number variation1nstd166human GRCh37.p13 chr17: 8,265,068-8,324,852 , GRCh38.p12 chr17: 8,361,750-8,421,534 KRBA2, RPL26, 1 more genes
    nsv3971181copy number variation1nstd168human GRCh38 chr17: 8,391,018-8,396,144 , GRCh37.p13 chr17: 8,294,336-8,299,462 RNF222
    nsv3965251insertion1nstd168human GRCh38 chr17: 8,377,985-8,412,869 , GRCh37.p13 chr17: 8,281,303-8,316,187 RPL26, RNF222
    nsv3923531copy number variation1nstd102humanPathogenic NCBI36 chr17: 7,322,238-8,279,567 , GRCh37 chr17: 7,381,514-8,338,842 , GRCh38 chr17: 7,478,195-8,435,524 SLC25A35, TRP-CGG1-3, 82 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3913608copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,871,030-8,393,597 , NCBI36 chr17: 7,811,755-8,334,322 , GRCh38 chr17: 7,967,712-8,490,279 AURKB, SNORD118, 47 more genes
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