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Items: 1 to 20 of 789

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953715insertion1nstd209human GRCh38 chr4: 86,969,879-86,969,879 , GRCh37.p13 chr4: 87,891,031-87,891,031 AFF1
    nsv5950171insertion1nstd209human GRCh38 chr4: 86,978,159-86,978,159 , GRCh37.p13 chr4: 87,899,311-87,899,311 AFF1
    nsv5903074copy number variation1nstd209human GRCh38 chr4: 87,095,601-87,095,861 , GRCh37.p13 chr4: 88,016,753-88,017,013 AFF1
    nsv5902289copy number variation1nstd209human GRCh38 chr4: 87,012,339-87,032,627 , GRCh37.p13 chr4: 87,933,491-87,953,779 AFF1
    nsv5900147copy number variation1nstd209human GRCh38 chr4: 86,972,042-86,972,094 , GRCh37.p13 chr4: 87,893,194-87,893,246 AFF1
    nsv5896467copy number variation1nstd209human GRCh38 chr4: 86,411,170-87,486,334 , GRCh37.p13 chr4: 87,332,323-88,407,486 , MIR4452, 21 more genes
    nsv5893621copy number variation1nstd209human GRCh38 chr4: 87,110,985-87,111,316 , GRCh37.p13 chr4: 88,032,137-88,032,468 AFF1
    nsv5840159copy number variation1nstd209human GRCh38 chr4: 87,012,404-87,021,771 , GRCh37.p13 chr4: 87,933,556-87,942,923 AFF1
    nsv5687096mobile element insertion2nstd211human GRCh38 chr4: 87,001,234-87,001,234 , GRCh37.p13 chr4: 87,922,386-87,922,386 AFF1
    nsv5682454mobile element insertion1nstd211human GRCh38 chr4: 86,947,901-86,947,901 , GRCh37.p13 chr4: 87,869,053-87,869,053 TECRP1, AFF1
    nsv5680759mobile element insertion2nstd211human GRCh38 chr4: 87,102,531-87,102,531 , GRCh37.p13 chr4: 88,023,683-88,023,683 AFF1
    nsv5679916mobile element insertion1nstd211human GRCh38 chr4: 86,982,417-86,982,417 , GRCh37.p13 chr4: 87,903,569-87,903,569 AFF1
    nsv5679902mobile element insertion1nstd211human GRCh38 chr4: 86,991,854-86,991,854 , GRCh37.p13 chr4: 87,913,006-87,913,006 AFF1
    nsv5570309copy number variation1nstd207human GRCh38 chr4: 87,110,985-87,111,316 , GRCh37.p13 chr4: 88,032,137-88,032,468 AFF1
    nsv5568905copy number variation1nstd207human GRCh38 chr4: 87,022,550-87,022,603 , GRCh37.p13 chr4: 87,943,702-87,943,755 AFF1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5470985copy number variation1nstd206human GRCh38 chr4: 87,075,813-87,076,156 , GRCh37.p13 chr4: 87,996,965-87,997,308 AFF1, LOC105377320
    nsv5464765copy number variation1nstd206human GRCh38 chr4: 87,111,003-87,111,317 , GRCh37.p13 chr4: 88,032,155-88,032,469 AFF1
    nsv5461903copy number variation1nstd206human GRCh38 chr4: 87,041,071-87,041,237 , GRCh37.p13 chr4: 87,962,223-87,962,389 AFF1
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