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Items: 1 to 20 of 126

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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
    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
    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
    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
    nsv5942682copy number variation1nstd209human GRCh38 chr17: 8,372,798-8,378,199 , GRCh37.p13 chr17: 8,276,116-8,281,517 RPL26, KRBA2
    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
    nsv5884609copy number variation1nstd209human GRCh38 chr17: 8,372,825-8,377,952 , GRCh37.p13 chr17: 8,276,143-8,281,270 KRBA2, RPL26
    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
    nsv5516696copy number variation1nstd206human GRCh38 chr17: 8,379,611-8,379,683 , GRCh37.p13 chr17: 8,282,929-8,283,001 RPL26
    nsv5374803translocation1nstd200human GRCh38 chr17: 8,376,122-8,376,122 , GRCh38 chr17: 8,378,028-8,378,028 , GRCh37.p13 chr17: 8,281,346-8,281,346 , GRCh37.p13 chr17: 8,279,440-8,279,440 KRBA2, RPL26
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4683837copy number variation2nstd102humanUncertain significance GRCh37 chr17: 8,131,488-8,285,638 , GRCh38.p12 chr17: 8,228,170-8,382,320 KRBA2, ARHGEF15, 7 more genes
    nsv4572799sequence alteration1nstd166human GRCh37.p13 chr17: 8,277,207-8,281,534 , GRCh38.p12 chr17: 8,373,889-8,378,216 RPL26, KRBA2
    nsv4457674copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,676,383-8,350,870 , GRCh38.p12 chr17: 7,773,065-8,447,552 ARHGEF15, TRI-AAT4-1, 57 more genes
    nsv4453653copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,572,917-8,285,638 , GRCh38 chr17: 7,669,599-8,382,320 TRS-AGA2-6, ODF4, 59 more genes
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