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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945361copy number variation1nstd209human GRCh38 chr17: 8,373,616-8,373,729 , GRCh37.p13 chr17: 8,276,934-8,277,047 KRBA2
    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
    nsv5721189mobile element insertion1nstd211human GRCh38 chr17: 8,370,886-8,370,886 , GRCh37.p13 chr17: 8,274,204-8,274,204 KRBA2
    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
    nsv5558362mobile element insertion1nstd206human GRCh38 chr17: 8,370,886-8,370,937 , GRCh37.p13 chr17: 8,274,204-8,274,255 KRBA2
    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
    nsv5187011mobile element insertion1nstd203human GRCh38 chr17: 8,370,870-8,370,886 , GRCh37.p13 chr17: 8,274,188-8,274,204 KRBA2
    nsv5146244mobile element insertion1nstd203human GRCh38 chr17: 8,374,937-8,374,937 , GRCh37.p13 chr17: 8,278,255-8,278,255 KRBA2
    nsv5145104mobile element insertion1nstd203human GRCh38 chr17: 8,374,915-8,374,937 , GRCh37.p13 chr17: 8,278,233-8,278,255 KRBA2
    nsv5140339mobile element insertion1nstd203human GRCh38 chr17: 8,374,904-8,374,937 , GRCh37.p13 chr17: 8,278,222-8,278,255 KRBA2
    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
    nsv4574016mobile element insertion1nstd166human GRCh37.p13 chr17: 8,274,188-8,274,188 , GRCh38.p12 chr17: 8,370,870-8,370,870 KRBA2
    nsv4573797mobile element insertion1nstd166human GRCh37.p13 chr17: 8,273,521-8,273,521 , GRCh38.p12 chr17: 8,370,203-8,370,203 KRBA2
    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
    nsv4249601copy number variation1nstd166human GRCh37.p13 chr17: 8,276,943-8,277,007 , GRCh38.p12 chr17: 8,373,625-8,373,689 KRBA2
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