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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5861339copy number variation1nstd209human GRCh38 chr9: 129,018,115-129,020,014 , GRCh37.p13 chr9: 131,780,394-131,782,293 SH3GLB2
    nsv5713220mobile element insertion1nstd211human GRCh38 chr9: 129,019,793-129,019,793 , GRCh37.p13 chr9: 131,782,072-131,782,072 SH3GLB2
    nsv5602694copy number variation1nstd207human GRCh38 chr9: 129,018,376-129,020,003 , GRCh37.p13 chr9: 131,780,655-131,782,282 SH3GLB2
    nsv5540131insertion1nstd206human GRCh38 chr9: 129,019,856-129,019,906 , GRCh37.p13 chr9: 131,782,135-131,782,185 SH3GLB2
    nsv5538764insertion1nstd206human GRCh38 chr9: 129,019,793-129,019,831 , GRCh37.p13 chr9: 131,782,072-131,782,110 SH3GLB2
    nsv5493899copy number variation1nstd206human GRCh38 chr9: 129,018,356-129,020,044 , GRCh37.p13 chr9: 131,780,635-131,782,323 SH3GLB2
    nsv5316623copy number variation1nstd204human GRCh38.p13 chr9: 129,018,416-129,019,966 , GRCh37.p13 chr9: 131,780,695-131,782,245 SH3GLB2
    nsv5310909copy number variation1nstd204human GRCh38.p13 chr9: 129,017,550-129,018,336 , GRCh37.p13 chr9: 131,779,829-131,780,615 SH3GLB2
    nsv5241889copy number variation1nstd204human GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379 , KYAT1, 32 more genes
    nsv5133709mobile element insertion1nstd203human GRCh38 chr9: 129,019,784-129,019,793 , GRCh37.p13 chr9: 131,782,063-131,782,072 SH3GLB2
    nsv5130770mobile element insertion1nstd203human GRCh38 chr9: 129,019,785-129,019,793 , GRCh37.p13 chr9: 131,782,064-131,782,072 SH3GLB2
    nsv5125286mobile element insertion1nstd203human GRCh38 chr9: 129,019,787-129,019,793 , GRCh37.p13 chr9: 131,782,066-131,782,072 SH3GLB2
    nsv5121454mobile element insertion1nstd203human GRCh38 chr9: 129,019,780-129,019,793 , GRCh37.p13 chr9: 131,782,059-131,782,072 SH3GLB2
    nsv4988432copy number variation1nstd200human GRCh38 chr9: 129,018,429-129,019,947 , GRCh37.p13 chr9: 131,780,708-131,782,226 SH3GLB2
    nsv4988431copy number variation1nstd200human GRCh38 chr9: 129,014,202-129,014,270 , GRCh37.p13 chr9: 131,776,481-131,776,549 SH3GLB2
    nsv4846061copy number variation1nstd200human GRCh37 chr9: 131,780,861-131,781,903 , GRCh38.p12 chr9: 129,018,582-129,019,624 SH3GLB2
    nsv4842497copy number variation1nstd200human GRCh37 chr9: 131,780,708-131,782,222 , GRCh38.p12 chr9: 129,018,429-129,019,943 SH3GLB2
    nsv4716709mobile element insertion1nstd186human GRCh37 chr9: 131,782,059-131,782,059 , GRCh38.p12 chr9: 129,019,780-129,019,780 SH3GLB2
    nsv4675731copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931 PTPA, GLE1, 55 more genes
    nsv4675555copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,094,304-131,863,858 , GRCh38.p12 chr9: 128,332,025-129,101,579 ENDOG, SPOUT1, 35 more genes
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