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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7095365copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-8,285,628 , GRCh38.p12 chr17: 7,668,434-8,382,310 TRK-TTT3-5, WRAP53, 59 more genes
    nsv7077200inversion1nstd229human GRCh38 chr17: 8,311,394-8,420,761 , GRCh37.p13 chr17: 8,214,712-8,324,079 LOC100128288, ARHGEF15, 4 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    nsv6991993copy number variation1nstd229human GRCh38 chr17: 8,355,610-8,358,344 , GRCh37.p13 chr17: 8,258,928-8,261,662 LOC100128288
    nsv6991925copy number variation1nstd229human GRCh38 chr17: 8,330,042-8,359,647 , GRCh37.p13 chr17: 8,233,360-8,262,965 LOC100128288, ODF4
    nsv6988892copy number variation1nstd229human GRCh38 chr17: 8,305,883-8,356,856 , GRCh37.p13 chr17: 8,209,201-8,260,174 LOC100128288, ARHGEF15, 1 more genes
    nsv6985599copy number variation1nstd229human GRCh38 chr17: 8,359,127-8,365,904 , GRCh37.p13 chr17: 8,262,445-8,269,222 LOC100128288
    nsv6982823copy number variation1nstd229human GRCh38 chr17: 8,148,126-8,376,847 , GRCh37.p13 chr17: 8,051,444-8,280,165 TRW-CCA1-1, TRG-TCC3-1, 27 more genes
    nsv6513806copy number variation1nstd223human GRCh38 chr17: 7,990,455-8,357,154 , GRCh37.p13 chr17: 7,893,773-8,260,472 TRR-TCT2-1, TRP-CGG1-3, 41 more genes
    nsv6310345copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,136,214-8,285,628 , GRCh38.p12 chr17: 8,232,896-8,382,310 PFAS, RPL26, 7 more genes
    nsv6310202copy number variation2nstd102humanUncertain significance GRCh37 chr17: 8,131,498-8,285,628 , GRCh38.p12 chr17: 8,228,180-8,382,310 CTC1, RANGRF, 7 more genes
    nsv6137346translocation1nstd213human GRCh37 chr17: 8,263,578-8,263,578 , GRCh38.p12 chr17: 8,360,260-8,360,260 , GRCh37 chr11: 46,131,352-46,131,352 , GRCh38.p12 chr11: 46,109,801-46,109,801 PHF21A, LOC100128288
    nsv6137330translocation1nstd213human GRCh37 chr17: 8,263,563-8,263,563 , GRCh38.p12 chr17: 8,360,245-8,360,245 , GRCh37 chr11: 46,131,352-46,131,352 , GRCh38.p12 chr11: 46,109,801-46,109,801 PHF21A, LOC100128288
    nsv6133065copy number variation1nstd213human GRCh37 chr17: 4,530,000-8,270,001 , GRCh38.p12 chr17: 4,626,705-8,366,683 ACADVL, ALOX12, 206 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    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
    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
    nsv5531700copy number variation1nstd206human GRCh38 chr17: 8,353,842-8,356,653 , GRCh37.p13 chr17: 8,257,160-8,259,971 LOC100128288
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