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Items: 1 to 20 of 165

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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
    nsv5153584mobile element insertion1nstd203human GRCh38 chr17: 8,452,226-8,452,240 , GRCh37.p13 chr17: 8,355,544-8,355,558 NDEL1
    nsv5148757mobile element insertion1nstd203human GRCh38 chr17: 8,461,830-8,461,840 , GRCh37.p13 chr17: 8,365,148-8,365,158 NDEL1
    nsv5015794copy number variation1nstd200human GRCh38 chr17: 8,473,053-8,474,360 , GRCh37.p13 chr17: 8,376,371-8,377,678 NDEL1, MYH10
    nsv5015793copy number variation1nstd200human GRCh38 chr17: 8,467,819-8,469,933 , GRCh37.p13 chr17: 8,371,137-8,373,251 NDEL1
    nsv4857982copy number variation1nstd200human GRCh37 chr17: 8,376,371-8,377,678 , GRCh38.p12 chr17: 8,473,053-8,474,360 NDEL1, MYH10
    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
    nsv4246150copy number variation1nstd166human GRCh37.p13 chr17: 8,341,825-8,341,914 , GRCh38.p12 chr17: 8,438,507-8,438,596 NDEL1
    nsv4244160copy number variation1nstd166human GRCh37.p13 chr17: 8,368,109-8,377,711 , GRCh38.p12 chr17: 8,464,791-8,474,393 MYH10, NDEL1
    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
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 SLC2A4, CCDC92B, 401 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3902311copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,929,776-9,995,862 , GRCh38.p12 chr17: 8,026,458-10,092,545 RCVRN, TRQ-CTG1-5, 74 more genes
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