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Items: 1 to 20 of 960

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097836copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,771,504-6,182,394 , GRCh38.p12 chr6: 5,771,271-6,182,161 RPL34P16, PKMP5, 8 more genes
    nsv7097835copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,404,755-5,431,425 , GRCh38.p12 chr6: 5,404,522-5,431,192 FARS2
    nsv7097834copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,368,804-5,369,435 , GRCh38.p12 chr6: 5,368,571-5,369,202 FARS2
    nsv7097833copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,216,831-5,431,425 , GRCh38.p12 chr6: 5,216,598-5,431,192 LYRM4, LYRM4-AS1, 1 more genes
    nsv7097573copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,368,804-5,613,573 , GRCh38.p12 chr6: 5,368,571-5,613,340 HNRNPA1P37, FARS2, 1 more genes
    nsv7097442copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,404,755-5,545,593 , GRCh38.p12 chr6: 5,404,522-5,545,360 FARS2, FARS2-AS1
    nsv7097441copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 5,404,755-5,404,954 , GRCh38.p12 chr6: 5,404,522-5,404,721 FARS2
    nsv7097440copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 5,368,804-5,404,954 , GRCh38.p12 chr6: 5,368,571-5,404,721 FARS2
    nsv7097336copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,109,657-6,320,826 , GRCh38.p12 chr6: 5,109,423-6,320,593 FARS2, LYRM4-AS1, 14 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7053511inversion1nstd229human GRCh38 chr6: 5,767,253-5,767,498 , GRCh37.p13 chr6: 5,767,486-5,767,731 FARS2
    nsv7051290inversion1nstd229human GRCh38 chr6: 5,358,916-5,380,805 , GRCh37.p13 chr6: 5,359,149-5,381,038 FARS2
    nsv7050925inversion1nstd229human GRCh38 chr6: 5,497,671-5,502,578 , GRCh37.p13 chr6: 5,497,904-5,502,811 FARS2
    nsv7049487inversion1nstd229human GRCh38 chr6: 5,024,985-5,441,289 , GRCh37.p13 chr6: 5,025,219-5,441,522 PPP1R3G, TFB2MP1, 4 more genes
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7047183inversion1nstd229human GRCh38 chr6: 5,572,878-5,578,400 , GRCh37.p13 chr6: 5,573,111-5,578,633 FARS2
    nsv7046068inversion1nstd229human GRCh38 chr6: 5,435,767-5,654,416 , GRCh37.p13 chr6: 5,436,000-5,654,649 FARS2, HNRNPA1P37, 1 more genes
    nsv7044709inversion1nstd229human GRCh38 chr6: 5,231,715-5,431,877 , GRCh37.p13 chr6: 5,231,948-5,432,110 LYRM4-AS1, FARS2, 1 more genes
    nsv7043753inversion1nstd229human GRCh38 chr6: 5,606,187-5,607,137 , GRCh37.p13 chr6: 5,606,420-5,607,370 FARS2, HNRNPA1P37
    nsv7039748inversion1nstd229human GRCh38 chr6: 5,365,864-5,365,937 , GRCh37.p13 chr6: 5,366,097-5,366,170 FARS2
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