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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125499copy number variation1nstd186human GRCh37 chr17: 6,770,022-6,770,333 , GRCh38.p12 chr17: 6,866,703-6,867,014 ALOX12P2
    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
    nsv5673052copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117 RPL23AP73, MIR195, 25 more genes
    nsv5586431copy number variation1nstd207human GRCh38 chr17: 6,866,690-6,867,013 , GRCh37.p13 chr17: 6,770,009-6,770,332 ALOX12P2
    nsv5529425copy number variation1nstd206human GRCh38 chr17: 6,866,703-6,867,014 , GRCh37.p13 chr17: 6,770,022-6,770,333 ALOX12P2
    nsv5520778copy number variation1nstd206human GRCh38 chr17: 6,892,890-6,892,959 , GRCh37.p13 chr17: 6,796,209-6,796,278 ALOX12P2
    nsv5520002copy number variation1nstd206human GRCh38 chr17: 6,872,684-6,872,868 , GRCh37.p13 chr17: 6,776,003-6,776,187 ALOX12P2
    nsv5515051copy number variation1nstd206human GRCh38 chr17: 6,851,686-6,851,857 , GRCh37.p13 chr17: 6,755,005-6,755,176 ALOX12P2
    nsv5384746mobile element deletion1nstd186human GRCh37 chr17: 6,770,022-6,770,333 , GRCh38.p12 chr17: 6,866,703-6,867,014 ALOX12P2
    nsv5381181copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,128,416 , GRCh38.p12 chr17: 6,425,460-7,225,097 RNA5SP435, RPL23AP73, 37 more genes
    nsv5299757copy number variation1nstd204human GRCh38.p13 chr17: 6,830,070-6,861,121 , GRCh37.p13 chr17: 6,733,389-6,764,440 TEKT1, ALOX12P2
    nsv5283044copy number variation1nstd204human GRCh38.p13 chr17: 6,882,862-6,883,932 , GRCh37.p13 chr17: 6,786,181-6,787,251 ALOX12P2
    nsv5206627mobile element deletion1nstd204human GRCh38.p13 chr17: 6,866,674-6,867,035 , GRCh37.p13 chr17: 6,769,993-6,770,354 ALOX12P2
    nsv5158509mobile element insertion1nstd203human GRCh38 chr17: 6,866,975-6,867,023 , GRCh37.p13 chr17: 6,770,294-6,770,342 ALOX12P2
    nsv5146812mobile element insertion1nstd203human GRCh38 chr17: 6,866,995-6,867,023 , GRCh37.p13 chr17: 6,770,314-6,770,342 ALOX12P2
    nsv5023612copy number variation1nstd200human GRCh38 chr17: 6,889,217-6,891,259 , GRCh37.p13 chr17: 6,792,536-6,794,578 ALOX12P2
    nsv5023611copy number variation1nstd200human GRCh38 chr17: 6,871,364-6,872,070 , GRCh37.p13 chr17: 6,774,683-6,775,389 ALOX12P2
    nsv5015699copy number variation1nstd200human GRCh38 chr17: 6,853,147-6,960,047 , GRCh37.p13 chr17: 6,756,466-6,863,366 SPICP3, ALOX12P2
    nsv5015695copy number variation1nstd200human GRCh38 chr17: 6,724,159-6,902,878 , GRCh37.p13 chr17: 6,627,478-6,806,197 FBXO39, RPL23AP73, 3 more genes
    nsv4907312mobile element deletion1nstd200human GRCh38 chr17: 6,866,703-6,867,014 , GRCh37.p13 chr17: 6,770,022-6,770,333 ALOX12P2
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