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Items: 1 to 20 of 221

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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
    nsv6991925copy number variation1nstd229human GRCh38 chr17: 8,330,042-8,359,647 , GRCh37.p13 chr17: 8,233,360-8,262,965 LOC100128288, ODF4
    nsv6991154copy number variation1nstd229human GRCh38 chr17: 8,343,327-8,344,685 , GRCh37.p13 chr17: 8,246,645-8,248,003 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
    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
    nsv6978459copy number variation1nstd229human GRCh38 chr17: 8,320,672-8,345,660 , GRCh37.p13 chr17: 8,223,990-8,248,978 ARHGEF15, ODF4
    nsv6515071copy number variation1nstd223human GRCh38 chr17: 8,331,016-8,339,362 , GRCh37.p13 chr17: 8,234,334-8,242,680 ODF4
    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
    nsv6508187copy number variation1nstd223human GRCh38 chr17: 8,343,335-8,344,650 , GRCh37.p13 chr17: 8,246,653-8,247,968 ODF4
    nsv6500952copy number variation1nstd223human GRCh38 chr17: 8,320,672-8,345,659 , GRCh37.p13 chr17: 8,223,990-8,248,977 ARHGEF15, ODF4
    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
    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
    nsv6129114copy number variation1nstd186human GRCh37 chr17: 8,246,653-8,247,968 , GRCh38.p12 chr17: 8,343,335-8,344,650 ODF4
    nsv6027163copy number variation1nstd212human GRCh38 chr17: 8,343,320-8,344,667 , GRCh37.p13 chr17: 8,246,638-8,247,985 ODF4
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