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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902580copy number variation1nstd209human GRCh38 chr6: 44,215,301-44,215,622 , GRCh37.p13 chr6: 44,183,038-44,183,359 MYMX
    nsv5897489copy number variation1nstd209human GRCh38 chr6: 44,213,339-44,213,489 , GRCh37.p13 chr6: 44,181,076-44,181,226 MYMX
    nsv5893129copy number variation1nstd209human GRCh38 chr6: 44,196,851-44,197,425 , GRCh37.p13 chr6: 44,164,588-44,165,162 MYMX
    nsv5716270mobile element insertion1nstd211human GRCh38 chr6: 44,202,443-44,202,443 , GRCh37.p13 chr6: 44,170,180-44,170,180 MYMX
    nsv5639028insertion1nstd207human GRCh38 chr6: 44,202,428-44,202,428 , GRCh37.p13 chr6: 44,170,165-44,170,165 MYMX
    nsv5569511copy number variation1nstd207human GRCh38 chr6: 44,196,851-44,197,425 , GRCh37.p13 chr6: 44,164,588-44,165,162 MYMX
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5471452copy number variation1nstd206human GRCh38 chr6: 44,213,320-44,213,510 , GRCh37.p13 chr6: 44,181,057-44,181,247 MYMX
    nsv5455797copy number variation1nstd206human GRCh38 chr6: 44,196,881-44,197,497 , GRCh37.p13 chr6: 44,164,618-44,165,234 MYMX
    nsv5314347copy number variation1nstd204human GRCh38.p13 chr6: 44,198,297-44,199,318 , GRCh37.p13 chr6: 44,166,034-44,167,055 MYMX
    nsv5311270copy number variation1nstd204human GRCh38.p13 chr6: 44,196,880-44,197,416 , GRCh37.p13 chr6: 44,164,617-44,165,153 MYMX
    nsv5181532mobile element insertion1nstd203human GRCh38 chr6: 44,202,428-44,202,443 , GRCh37.p13 chr6: 44,170,165-44,170,180 MYMX
    nsv5180597mobile element insertion1nstd203human GRCh38 chr6: 44,202,443-44,202,443 , GRCh37.p13 chr6: 44,170,180-44,170,180 MYMX
    nsv4941174copy number variation1nstd200human GRCh38 chr6: 44,213,342-44,213,490 , GRCh37.p13 chr6: 44,181,079-44,181,227 MYMX
    nsv4941173copy number variation1nstd200human GRCh38 chr6: 44,210,037-44,213,461 , GRCh37.p13 chr6: 44,177,774-44,181,198 RN7SL811P, MYMX
    nsv4941172copy number variation1nstd200human GRCh38 chr6: 44,209,237-44,209,368 , GRCh37.p13 chr6: 44,176,974-44,177,105 RN7SL811P, MYMX
    nsv4816217copy number variation1nstd200human GRCh37 chr6: 44,177,774-44,181,198 , GRCh38.p12 chr6: 44,210,037-44,213,461 RN7SL811P, MYMX
    nsv4816216copy number variation1nstd200human GRCh37 chr6: 44,166,043-44,167,048 , GRCh38.p12 chr6: 44,198,306-44,199,311 MYMX
    nsv4816215copy number variation1nstd200human GRCh37 chr6: 44,164,632-44,165,127 , GRCh38.p12 chr6: 44,196,895-44,197,390 MYMX
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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