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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
    nsv5942682copy number variation1nstd209human GRCh38 chr17: 8,372,798-8,378,199 , GRCh37.p13 chr17: 8,276,116-8,281,517 RPL26, KRBA2
    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
    nsv5884609copy number variation1nstd209human GRCh38 chr17: 8,372,825-8,377,952 , GRCh37.p13 chr17: 8,276,143-8,281,270 KRBA2, RPL26
    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
    nsv5516696copy number variation1nstd206human GRCh38 chr17: 8,379,611-8,379,683 , GRCh37.p13 chr17: 8,282,929-8,283,001 RPL26
    nsv5374803translocation1nstd200human GRCh38 chr17: 8,376,122-8,376,122 , GRCh38 chr17: 8,378,028-8,378,028 , GRCh37.p13 chr17: 8,281,346-8,281,346 , GRCh37.p13 chr17: 8,279,440-8,279,440 KRBA2, RPL26
    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
    nsv4572799sequence alteration1nstd166human GRCh37.p13 chr17: 8,277,207-8,281,534 , GRCh38.p12 chr17: 8,373,889-8,378,216 RPL26, KRBA2
    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
    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
    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
    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
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