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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959466insertion1nstd209human GRCh38 chr3: 57,212,557-57,212,557 , GRCh37.p13 chr3: 57,246,585-57,246,585 HESX1
    nsv5690167mobile element insertion1nstd211human GRCh38 chr3: 57,196,869-57,196,869 , GRCh37.p13 chr3: 57,230,897-57,230,897 HESX1
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5188996mobile element insertion1nstd203human GRCh38 chr3: 57,196,841-57,196,856 , GRCh37.p13 chr3: 57,230,869-57,230,884 HESX1
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4794009copy number variation1nstd200human GRCh37 chr3: 57,236,136-57,242,684 , GRCh38.p12 chr3: 57,202,108-57,208,656 HESX1
    nsv4790814copy number variation1nstd200human GRCh37 chr3: 57,252,414-57,253,192 , GRCh38.p12 chr3: 57,218,386-57,219,164 HESX1
    nsv4680494copy number variation1nstd189human GRCh37.p13 chr3: 57,093,803-57,495,890 , GRCh38.p12 chr3: 57,059,775-57,510,163 HESX1, APPL1, 8 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv4080444copy number variation1nstd166human GRCh37.p13 chr3: 57,228,872-57,230,105 , GRCh38.p12 chr3: 57,194,844-57,196,077 HESX1
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 MAGI1-AS1, FEZF2, 135 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3875047copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483 SLMAP, SNORD19C, 132 more genes
    nsv3168877copy number variation1nstd158human GRCh37 chr3: 38,483,456-71,473,806 , GRCh38.p12 chr3: 38,441,965-71,424,655 , ACVR2B, 646 more genes
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