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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7097431copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,141,352-42,141,572 , GRCh38.p12 chr6: 42,173,614-42,173,834 GUCA1A
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv6789272copy number variation1nstd229human GRCh38 chr6: 41,897,601-42,523,500 , GRCh37.p13 chr6: 41,865,339-42,491,238 LOC105375061, RPL36AP5, 13 more genes
    nsv6783886copy number variation1nstd229human GRCh38 chr6: 42,163,065-42,171,589 , GRCh37.p13 chr6: 42,130,803-42,139,327 GUCA1A, CIMIP3
    nsv6781340copy number variation1nstd229human GRCh38 chr6: 42,174,684-42,175,090 , GRCh37.p13 chr6: 42,142,422-42,142,828 GUCA1A
    nsv6780727copy number variation1nstd229human GRCh38 chr6: 42,161,045-42,162,104 , GRCh37.p13 chr6: 42,128,783-42,129,842 GUCA1A, CIMIP3
    nsv6636814copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,043,510-42,274,148 , GRCh38.p12 chr6: 42,075,772-42,306,410 TRERF1, LOC105375061, 6 more genes
    nsv6631499copy number variation1nstd224human GRCh37 chr6: 42,074,371-42,153,535 , GRCh38.p12 chr6: 42,106,633-42,185,797 GUCA1A, C6orf132, 2 more genes
    nsv6410990copy number variation1nstd223human GRCh38 chr6: 42,160,965-42,162,190 , GRCh37.p13 chr6: 42,128,703-42,129,928 GUCA1A, CIMIP3
    nsv6397647copy number variation1nstd223human GRCh38 chr6: 42,168,030-42,168,477 , GRCh37.p13 chr6: 42,135,768-42,136,215 GUCA1A
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6002039copy number variation1nstd212human GRCh38 chr6: 42,160,965-42,162,190 , GRCh37.p13 chr6: 42,128,703-42,129,928 CIMIP3, GUCA1A
    nsv5891802copy number variation1nstd209human GRCh38 chr6: 42,160,965-42,162,189 , GRCh37.p13 chr6: 42,128,703-42,129,927 CIMIP3, GUCA1A
    nsv5692443mobile element insertion1nstd211human GRCh38 chr6: 42,153,981-42,153,981 , GRCh37.p13 chr6: 42,121,719-42,121,719 CIMIP3, GUCA1A
    nsv5636160insertion1nstd207human GRCh38 chr6: 42,153,965-42,153,965 , GRCh37.p13 chr6: 42,121,703-42,121,703 GUCA1A, CIMIP3
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5470547copy number variation1nstd206human GRCh38 chr6: 42,160,993-42,162,141 , GRCh37.p13 chr6: 42,128,731-42,129,879 GUCA1A, CIMIP3
    nsv5462700copy number variation1nstd206human GRCh38 chr6: 42,175,804-42,188,280 , GRCh37.p13 chr6: 42,143,542-42,156,018 GUCA1B, GUCA1A
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