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Items: 1 to 20 of 107

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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
    nsv6988871copy number variation1nstd229human GRCh38 chr17: 29,612,301-29,618,200 , GRCh37.p13 chr17: 27,939,319-27,945,218 CORO6, ANKRD13B
    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
    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
    nsv5875934copy number variation1nstd209human GRCh38 chr17: 29,604,701-29,614,445 , GRCh37.p13 chr17: 27,931,719-27,941,463 ANKRD13B, CORO6
    nsv4864596copy number variation1nstd200human GRCh37 chr17: 27,867,683-28,200,332 , GRCh38.p12 chr17: 29,540,665-29,873,314 ANKRD13B, TAOK1, 10 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729763copy number variation1nstd102humanUncertain significance GRCh37 chr17: 27,573,641-28,206,747 , GRCh38.p12 chr17: 29,246,623-29,879,729 GIT1, RPL21P123, 17 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4370646copy number variation1nstd173human GRCh37 chr17: 27,870,962-28,495,223 , GRCh38.p12 chr17: 29,543,944-30,168,205 RNU6-920P, ABHD15, 16 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4236689copy number variation1nstd166human GRCh37.p13 chr17: 27,940,911-27,940,970 , GRCh38.p12 chr17: 29,613,893-29,613,952 ANKRD13B, CORO6
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