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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146754copy number variation1nstd232human GRCh37.p13 chr3: 57,320,418-57,320,492 , GRCh38.p12 chr3: 57,286,390-57,286,464 ASB14
    nsv7097210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,130,421-58,520,833 , GRCh38.p12 chr3: 57,096,393-58,535,106 LOC107984079, SLMAP, 37 more genes
    nsv7097209copy number variation1nstd102humanUncertain significance GRCh37 chr3: 57,130,421-57,303,715 , GRCh38.p12 chr3: 57,096,393-57,269,687 APPL1, LOC105377102, 5 more genes
    nsv7051968inversion1nstd229human GRCh38 chr3: 56,944,702-65,952,705 , GRCh37.p13 chr3: 56,978,730-65,938,380 ILF2P1, ARHGEF3-AS1, 115 more genes
    nsv7044401inversion1nstd229human GRCh38 chr3: 57,281,537-57,281,624 , GRCh37.p13 chr3: 57,315,565-57,315,652 ASB14
    nsv7038236inversion1nstd229human GRCh38 chr3: 56,950,550-57,362,669 , GRCh37.p13 chr3: 56,984,578-57,369,477 SPATA12, APPL1, 9 more genes
    nsv6716141copy number variation1nstd229human GRCh38 chr3: 57,288,899-57,294,515 , GRCh37.p13 chr3: 57,322,927-57,328,543 DNAH12, ASB14
    nsv6711757copy number variation1nstd229human GRCh38 chr3: 57,243,901-57,267,300 , GRCh37.p13 chr3: 57,277,929-57,301,328 APPL1, ASB14
    nsv6709009copy number variation1nstd229human GRCh38 chr3: 57,265,277-57,313,178 , GRCh37.p13 chr3: 57,299,305-57,347,206 APPL1, DNAH12, 2 more genes
    nsv6701712copy number variation1nstd229human GRCh38 chr3: 57,231,818-57,402,279 , GRCh37.p13 chr3: 57,265,846-57,369,477 ASB14, DNAH12, 2 more genes
    nsv6699784copy number variation1nstd229human GRCh38 chr3: 57,286,394-57,286,465 , GRCh37.p13 chr3: 57,320,422-57,320,493 ASB14
    nsv6373089copy number variation1nstd223human GRCh38 chr3: 57,286,978-57,287,609 , GRCh37.p13 chr3: 57,321,006-57,321,637 ASB14
    nsv6363660copy number variation1nstd223human GRCh38 chr3: 57,288,898-57,294,515 , GRCh37.p13 chr3: 57,322,926-57,328,543 DNAH12, ASB14
    nsv6359243copy number variation1nstd223human GRCh38 chr3: 57,286,390-57,286,465 , GRCh37.p13 chr3: 57,320,418-57,320,493 ASB14
    nsv6149166copy number variation1nstd214human GRCh38 chr3: 57,286,390-57,286,464 , GRCh37.p13 chr3: 57,320,418-57,320,492 ASB14
    nsv6135018copy number variation1nstd213human GRCh37 chr3: 56,590,000-58,400,001 , GRCh38.p12 chr3: 56,555,972-58,414,274 ARF4, DNASE1L3, 36 more genes
    nsv5888580copy number variation1nstd209human GRCh38 chr3: 57,286,390-57,286,464 , GRCh37.p13 chr3: 57,320,418-57,320,492 ASB14
    nsv5674411mobile element insertion1nstd211human GRCh38 chr3: 57,280,186-57,280,186 , GRCh37.p13 chr3: 57,314,214-57,314,214 ASB14
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5351797translocation1nstd200human GRCh38 chr3: 57,286,465-57,286,465 , GRCh38 chr3: 57,286,394-57,286,394 , GRCh37.p13 chr3: 57,320,422-57,320,422 , GRCh37.p13 chr3: 57,320,493-57,320,493 ASB14
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