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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6995041copy number variation1nstd229human GRCh38 chr17: 29,590,307-29,592,801 , GRCh37.p13 chr17: 27,917,325-27,919,819 ANKRD13B
    nsv6988871copy number variation1nstd229human GRCh38 chr17: 29,612,301-29,618,200 , GRCh37.p13 chr17: 27,939,319-27,945,218 CORO6, ANKRD13B
    nsv6987333copy number variation1nstd229human GRCh38 chr17: 29,606,631-29,606,952 , GRCh37.p13 chr17: 27,933,649-27,933,970 ANKRD13B
    nsv6985838copy number variation1nstd229human GRCh38 chr17: 29,564,843-29,589,650 , GRCh37.p13 chr17: 27,891,861-27,916,668 ANKRD13B, ABHD15, 2 more genes
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6980148copy number variation1nstd229human GRCh38 chr17: 29,597,764-29,598,221 , GRCh37.p13 chr17: 27,924,782-27,925,239 ANKRD13B
    nsv6508314copy number variation1nstd223human GRCh38 chr17: 29,606,645-29,606,939 , GRCh37.p13 chr17: 27,933,663-27,933,957 ANKRD13B
    nsv6502937copy number variation1nstd223human GRCh38 chr17: 29,564,843-29,589,650 , GRCh37.p13 chr17: 27,891,861-27,916,668 TP53I13, ABHD15, 2 more genes
    nsv6314364complex chromosomal rearrangement2nstd102humanUncertain significance GRCh37 chr17: 27,924,463-27,924,463 , GRCh37 chr17: 27,924,465-27,924,465 , GRCh38.p12 chr17: 29,597,445-29,597,445 , GRCh38.p12 chr17: 29,597,447-29,597,447 , GRCh38.p12 chr12: 51,875,884-51,875,884 , GRCh38.p12 chr12: 51,875,890-51,875,890 , GRCh37 chr12: 52,269,668-52,269,668 , GRCh37 chr12: 52,269,674-52,269,674 ANKRD13B
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6133298copy number variation1nstd213human GRCh37 chr17: 27,880,000-28,800,001 , GRCh38.p12 chr17: 29,552,982-30,472,983 BLMH, CPD, 23 more genes
    nsv6133234copy number variation1nstd213human GRCh37 chr17: 27,810,000-28,370,001 , GRCh38.p12 chr17: 29,482,982-30,042,983 TP53I13, ABHD15, 11 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv5944562copy number variation1nstd209human GRCh38 chr17: 29,540,718-29,873,240 , GRCh37.p13 chr17: 27,867,736-28,200,258 RPL21P123, GIT1, 10 more genes
    nsv5876132copy number variation1nstd209human GRCh38 chr17: 29,589,861-29,603,324 , GRCh37.p13 chr17: 27,916,879-27,930,342 GIT1, ANKRD13B
    nsv5875934copy number variation1nstd209human GRCh38 chr17: 29,604,701-29,614,445 , GRCh37.p13 chr17: 27,931,719-27,941,463 ANKRD13B, CORO6
    nsv5523230copy number variation1nstd206human GRCh38 chr17: 29,606,631-29,606,952 , GRCh37.p13 chr17: 27,933,649-27,933,970 ANKRD13B
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