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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053306inversion1nstd229human GRCh38 chr5: 181,249,803-181,279,104 , GRCh37.p13 chr5: 180,676,803-180,706,105 TRIM52, TRIM52-AS1, 1 more genes
    nsv7045576inversion1nstd229human GRCh38 chr5: 180,805,627-181,281,045 , GRCh37.p13 chr5: 180,232,627-180,708,046 RPL13P10, TRV-AAC1-3, 46 more genes
    nsv7044684inversion1nstd229human GRCh38 chr5: 181,222,491-181,283,985 , GRCh37.p13 chr5: 180,649,491-180,710,986 TRV-CAC1-5, TRIM52, 8 more genes
    nsv7044540inversion1nstd229human GRCh38 chr5: 180,832,761-181,281,244 , GRCh37.p13 chr5: 180,259,761-180,708,245 LOC100128762, SNORD95, 44 more genes
    nsv6792730copy number variation1nstd229human GRCh38 chr5: 181,272,512-181,286,322 , GRCh37.p13 chr5: 180,699,513-180,713,323 TRIM52-AS1
    nsv6788959copy number variation1nstd229human GRCh38 chr5: 181,100,901-181,281,600 , GRCh37.p13 chr5: 180,527,901-180,708,601 TRV-AAC1-4, TRV-AAC1-2, 30 more genes
    nsv6788627copy number variation1nstd229human GRCh38 chr5: 181,266,528-181,270,340 , GRCh37.p13 chr5: 180,693,529-180,697,341 TRIM52-AS1
    nsv6787779copy number variation1nstd229human GRCh38 chr5: 181,257,340-181,272,261 , GRCh37.p13 chr5: 180,684,341-180,699,262 CTC-338M12.4, TRIM52-AS1, 1 more genes
    nsv6781945copy number variation1nstd229human GRCh38 chr5: 181,252,430-181,260,461 , GRCh37.p13 chr5: 180,679,430-180,687,462 TRIM52, TRIM52-AS1, 1 more genes
    nsv6779703copy number variation1nstd229human GRCh38 chr5: 181,244,127-181,288,038 , GRCh37.p13 chr5: 180,671,127-180,715,039 RACK1, TRIM52, 2 more genes
    nsv6636455copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,148,276-180,719,789 , GRCh38.p12 chr5: 180,721,276-181,292,788 OR2Y1, TRV-AAC1-2, 48 more genes
    nsv6635774copy number variation1nstd227human GRCh37 chr5: 180,682,862-180,693,127 , GRCh38.p12 chr5: 181,255,861-181,266,126 TRIM52, TRIM52-AS1, 1 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630143copy number variation1nstd224human GRCh37 chr5: 180,535,802-180,687,526 , GRCh38.p12 chr5: 181,108,802-181,260,525 TRP-TGG3-1, TRV-AAC1-4, 27 more genes
    nsv6566500inversion1nstd223human GRCh38 chr5: 181,249,803-181,279,104 , GRCh37.p13 chr5: 180,676,803-180,706,105 TRIM52, TRIM52-AS1, 1 more genes
    nsv6413193copy number variation1nstd223human GRCh38 chr5: 181,234,916-181,279,833 , GRCh37.p13 chr5: 180,661,916-180,706,834 RACK1, TRIM41, 5 more genes
    nsv6408274copy number variation1nstd223human GRCh38 chr5: 180,927,801-181,343,300 , GRCh37.p13 chr5: 180,354,801-180,770,301 TRK-CTT2-2, ARPP19P1, 47 more genes
    nsv6407330copy number variation1nstd223human GRCh38 chr5: 181,272,645-181,273,277 , GRCh37.p13 chr5: 180,699,646-180,700,278 TRIM52-AS1
    nsv6399064copy number variation1nstd223human GRCh38 chr5: 180,956,101-181,297,100 , GRCh37.p13 chr5: 180,383,101-180,724,101 FOXO1B, CTC-338M12.4, 40 more genes
    nsv6396360copy number variation1nstd223human GRCh38 chr5: 181,264,933-181,268,286 , GRCh37.p13 chr5: 180,691,934-180,695,287 TRIM52-AS1
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