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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5906945copy number variation1nstd209human GRCh38 chr6: 123,301,756-132,349,395 , GRCh37.p13 chr6: 123,622,901-132,670,534 , LOC105377999, 105 more genes
    nsv5903078copy number variation1nstd209human GRCh38 chr6: 127,138,998-127,139,076 , GRCh37.p13 chr6: 127,460,143-127,460,221 RSPO3
    nsv5898512copy number variation1nstd209human GRCh38 chr6: 127,176,550-127,176,615 , GRCh37.p13 chr6: 127,497,695-127,497,760 , RSPO3
    nsv5722981mobile element insertion2nstd211human GRCh38 chr6: 127,123,254-127,123,254 , GRCh37.p13 chr6: 127,444,399-127,444,399 RSPO3
    nsv5472964copy number variation1nstd206human GRCh38 chr6: 127,176,550-127,176,619 , GRCh37.p13 chr6: 127,497,695-127,497,764 , RSPO3
    nsv5468380copy number variation1nstd206human GRCh38 chr6: 127,139,539-127,139,590 , GRCh37.p13 chr6: 127,460,684-127,460,735 RSPO3
    nsv5458832copy number variation1nstd206human GRCh38 chr6: 126,370,926-127,424,730 , GRCh37.p13 chr6: 126,692,072-127,745,875 , YWHAZP4, 19 more genes
    nsv5456056copy number variation1nstd206human GRCh38 chr6: 127,139,555-127,139,619 , GRCh37.p13 chr6: 127,460,700-127,460,764 RSPO3
    nsv5369742translocation1nstd200human GRCh38 chr6: 127,176,550-127,176,550 , GRCh38 chr6: 127,176,619-127,176,619 , GRCh37.p13 chr6: 127,497,695-127,497,695 , GRCh37.p13 chr6: 127,497,764-127,497,764 , RSPO3
    nsv5324004translocation1nstd204human GRCh37.p13 chr6: 127,497,695-127,497,695 , GRCh37.p13 chr6: 127,497,764-127,497,764 , GRCh38.p13 chr6: 127,176,550-127,176,550 , GRCh38.p13 chr6: 127,176,619-127,176,619 , RSPO3
    nsv5224904copy number variation1nstd204human GRCh38.p13 chr6: 127,156,701-127,159,400 , GRCh37.p13 chr6: 127,477,846-127,480,545 RSPO3
    nsv5170528mobile element insertion1nstd203human GRCh38 chr6: 127,155,495-127,155,508 , GRCh37.p13 chr6: 127,476,640-127,476,653 RSPO3
    nsv5118374mobile element insertion1nstd203human GRCh38 chr6: 127,184,930-127,184,941 , GRCh37.p13 chr6: 127,506,075-127,506,086 , RSPO3
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4826375copy number variation1nstd200human GRCh37 chr6: 127,478,928-127,481,374 , GRCh38.p12 chr6: 127,157,783-127,160,229 RSPO3
    nsv4729286copy number variation1nstd102humanUncertain significance GRCh37 chr6: 127,289,665-127,570,560 , GRCh38.p12 chr6: 126,968,520-127,249,415 RSPO3, LOC105377989
    nsv4490260mobile element insertion1nstd166human GRCh37.p13 chr6: 127,449,470-127,449,470 , GRCh38.p12 chr6: 127,128,325-127,128,325 RSPO3
    nsv4488878mobile element insertion1nstd166human GRCh37.p13 chr6: 127,494,404-127,494,404 , GRCh38.p12 chr6: 127,173,259-127,173,259 , RSPO3
    nsv4488594mobile element insertion1nstd166human GRCh37.p13 chr6: 127,490,690-127,490,690 , GRCh38.p12 chr6: 127,169,545-127,169,545 RSPO3
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