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Items: 1 to 20 of 385

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968909inversion1nstd209human GRCh38 chr4: 184,990,077-186,324,974 , GRCh37.p13 chr4: 185,911,231-187,246,128 SLC25A4, F11, 25 more genes
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5903072copy number variation1nstd209human GRCh38 chr4: 186,008,703-186,213,064 , GRCh37.p13 chr4: 186,929,857-187,134,218 TLR3, FAM149A, 5 more genes
    nsv5893317copy number variation1nstd209human GRCh38 chr4: 186,081,212-186,082,167 , GRCh37.p13 chr4: 187,002,366-187,003,321 TLR3
    nsv5838821copy number variation1nstd209human GRCh38 chr4: 186,076,599-186,113,014 , GRCh37.p13 chr4: 186,997,753-187,034,168 FAM149A, TLR3
    nsv5838508copy number variation1nstd209human GRCh38 chr4: 186,008,121-186,073,607 , GRCh37.p13 chr4: 186,929,275-186,994,761 RNU4-64P, TLR3
    nsv5673650copy number variation1nstd102humanPathogenic GRCh37 chr4: 186,997,774-187,630,981 , GRCh38.p12 chr4: 186,076,620-186,709,827 FLJ38576, SLC25A5P6, 13 more genes
    nsv5472030copy number variation1nstd206human GRCh38 chr4: 186,081,212-186,082,168 , GRCh37.p13 chr4: 187,002,366-187,003,322 TLR3
    nsv5307443copy number variation1nstd204human GRCh38.p13 chr4: 185,946,317-186,402,737 , GRCh37.p13 chr4: 186,867,471-187,323,891 LTO1P1, RPSAP70, 10 more genes
    nsv5228065copy number variation1nstd204human GRCh38.p13 chr4: 186,062,599-186,103,084 , GRCh37.p13 chr4: 186,983,753-187,024,238 TLR3, FAM149A
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    nsv5034969inversion1nstd200human GRCh38 chr4: 185,525,494-188,054,826 , GRCh37.p13 chr4: 186,446,648-188,975,980 , F11-AS1, 34 more genes
    nsv4944147copy number variation1nstd200human GRCh38 chr4: 186,081,093-186,092,256 , GRCh37.p13 chr4: 187,002,247-187,013,410 TLR3
    nsv4944146copy number variation1nstd200human GRCh38 chr4: 186,060,807-186,136,943 , GRCh37.p13 chr4: 186,981,961-187,058,097 TLR3, FAM149A
    nsv4944145copy number variation1nstd200human GRCh38 chr4: 186,008,703-186,213,068 , GRCh37.p13 chr4: 186,929,857-187,134,222 FAM149A, CYP4V2, 5 more genes
    nsv4930532copy number variation1nstd200human GRCh38 chr4: 186,081,288-186,082,204 , GRCh37.p13 chr4: 187,002,442-187,003,358 TLR3
    nsv4930531copy number variation1nstd200human GRCh38 chr4: 186,073,479-186,076,021 , GRCh37.p13 chr4: 186,994,633-186,997,175 TLR3
    nsv4802140copy number variation1nstd200human GRCh37 chr4: 187,002,440-187,003,352 , GRCh38.p12 chr4: 186,081,286-186,082,198 TLR3
    nsv4802139copy number variation1nstd200human GRCh37 chr4: 186,994,633-186,997,175 , GRCh38.p12 chr4: 186,073,479-186,076,021 TLR3
    nsv4794754copy number variation1nstd200human GRCh37 chr4: 186,929,857-187,134,222 , GRCh38.p12 chr4: 186,008,703-186,213,068 TLR3, FAM149A, 5 more genes
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