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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5585607copy number variation1nstd207human GRCh38 chr10: 97,398,052-97,398,352 , GRCh37.p13 chr10: 99,157,809-99,158,109 RRP12
    nsv5475902copy number variation1nstd206human GRCh38 chr10: 97,398,013-97,398,376 , GRCh37.p13 chr10: 99,157,770-99,158,133 RRP12
    nsv5413289mobile element insertion1nstd206human GRCh38 chr10: 97,375,624-97,375,675 , GRCh37.p13 chr10: 99,135,381-99,135,432 RRP12
    nsv5384144mobile element deletion1nstd186human GRCh37 chr10: 99,157,822-99,158,110 , GRCh38.p12 chr10: 97,398,065-97,398,353 RRP12
    nsv5382535mobile element deletion1nstd186human GRCh37 chr10: 99,157,821-99,158,110 , GRCh38.p12 chr10: 97,398,064-97,398,353 RRP12
    nsv5365051translocation1nstd200human GRCh38 chr10: 97,385,257-97,385,257 , GRCh38 chr10: 97,388,251-97,388,251 , GRCh37.p13 chr10: 99,145,014-99,145,014 , GRCh37.p13 chr10: 99,148,008-99,148,008 RRP12
    nsv5348027translocation1nstd200human GRCh38 chr10: 97,388,626-97,388,626 , GRCh38 chr10: 97,390,422-97,390,422 , GRCh37.p13 chr10: 99,148,383-99,148,383 , GRCh37.p13 chr10: 99,150,179-99,150,179 RRP12
    nsv5348026translocation1nstd200human GRCh38 chr10: 97,372,072-97,372,072 , GRCh38 chr10: 97,371,083-97,371,083 , GRCh37.p13 chr10: 99,131,829-99,131,829 , GRCh37.p13 chr10: 99,130,840-99,130,840 RRP12
    nsv5345268translocation1nstd200human GRCh37 chr10: 99,145,014-99,145,014 , GRCh37 chr10: 99,148,008-99,148,008 , GRCh38.p12 chr10: 97,388,251-97,388,251 , GRCh38.p12 chr10: 97,385,257-97,385,257 RRP12
    nsv5340386translocation1nstd200human GRCh37 chr10: 99,148,383-99,148,383 , GRCh37 chr10: 99,150,179-99,150,179 , GRCh38.p12 chr10: 97,388,626-97,388,626 , GRCh38.p12 chr10: 97,390,422-97,390,422 RRP12
    nsv5339577translocation1nstd200human GRCh37 chr10: 99,130,840-99,130,840 , GRCh37 chr10: 99,131,829-99,131,829 , GRCh38.p12 chr10: 97,371,083-97,371,083 , GRCh38.p12 chr10: 97,372,072-97,372,072 RRP12
    nsv5337562translocation1nstd200human GRCh37 chr10: 99,133,331-99,133,331 , GRCh37 chr10: 99,132,960-99,132,960 , GRCh38.p12 chr10: 97,373,574-97,373,574 , GRCh38.p12 chr10: 97,373,203-97,373,203 RRP12
    nsv5258274copy number variation1nstd204human GRCh38.p13 chr10: 97,348,801-97,424,400 , GRCh37.p13 chr10: 99,108,558-99,184,157 RRP12, LOC644215, 2 more genes
    nsv5242174copy number variation1nstd204human GRCh38.p13 chr10: 97,398,001-97,398,400 , GRCh37.p13 chr10: 99,157,758-99,158,157 RRP12
    nsv5205966mobile element deletion1nstd204human GRCh38.p13 chr10: 97,398,059-97,398,360 , GRCh37.p13 chr10: 99,157,816-99,158,117 RRP12
    nsv5198569mobile element insertion1nstd203human GRCh38 chr10: 97,383,059-97,383,077 , GRCh37.p13 chr10: 99,142,816-99,142,834 RRP12
    nsv5137375mobile element insertion1nstd203human GRCh38 chr10: 97,371,370-97,371,387 , GRCh37.p13 chr10: 99,131,127-99,131,144 RRP12
    nsv5121149mobile element insertion1nstd203human GRCh38 chr10: 97,392,650-97,392,664 , GRCh37.p13 chr10: 99,152,407-99,152,421 RPL34P20, RRP12
    nsv4986855copy number variation1nstd200human GRCh38 chr10: 97,386,838-97,394,974 , GRCh37.p13 chr10: 99,146,595-99,154,731 RPL34P20, RRP12
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