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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5564399copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,192,101-8,283,260 , GRCh38.p12 chr17: 8,288,783-8,379,942 RANGRF, KRBA2, 5 more genes
    nsv5287366copy number variation1nstd204human GRCh38.p13 chr17: 8,146,701-8,295,100 , GRCh37.p13 chr17: 8,050,019-8,198,418 TMEM107, MIR4521, 22 more genes
    nsv5015778copy number variation1nstd200human GRCh38 chr17: 8,287,098-8,288,705 , GRCh37.p13 chr17: 8,190,416-8,192,023 RANGRF, SLC25A35
    nsv5015777copy number variation1nstd200human GRCh38 chr17: 8,278,672-8,303,809 , GRCh37.p13 chr17: 8,181,990-8,207,127 SLC25A35, RANGRF
    nsv5015775copy number variation1nstd200human GRCh38 chr17: 8,268,958-8,288,147 , GRCh37.p13 chr17: 8,172,276-8,191,465 PFAS, SLC25A35, 1 more genes
    nsv4857970copy number variation1nstd200human GRCh37 chr17: 8,190,417-8,192,023 , GRCh38.p12 chr17: 8,287,099-8,288,705 RANGRF, SLC25A35
    nsv4857969copy number variation1nstd200human GRCh37 chr17: 8,181,991-8,207,127 , GRCh38.p12 chr17: 8,278,673-8,303,809 SLC25A35, RANGRF
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4683837copy number variation2nstd102humanUncertain significance GRCh37 chr17: 8,131,488-8,285,638 , GRCh38.p12 chr17: 8,228,170-8,382,320 KRBA2, ARHGEF15, 7 more genes
    nsv4675487copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,937,691-8,247,776 , GRCh38.p12 chr17: 8,034,373-8,344,458 RANGRF, TRS-CGA1-1, 39 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
    nsv4453653copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,572,917-8,285,638 , GRCh38 chr17: 7,669,599-8,382,320 TRS-AGA2-6, ODF4, 59 more genes
    nsv4247328copy number variation1nstd166human GRCh37.p13 chr17: 8,181,991-8,207,127 , GRCh38.p12 chr17: 8,278,673-8,303,809 RANGRF, SLC25A35
    nsv4244354copy number variation1nstd166human GRCh37.p13 chr17: 8,106,185-8,201,284 , GRCh38.p12 chr17: 8,202,867-8,297,966 RANGRF, TRD-GTC2-11, 11 more genes
    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
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 more genes
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