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Items: 1 to 20 of 376

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5950031insertion1nstd209human GRCh38 chr4: 140,362,274-140,362,274 , GRCh37.p13 chr4: 141,283,428-141,283,428 SCOC, SCOC-AS1
    nsv5901303copy number variation1nstd209human GRCh38 chr4: 140,302,934-140,302,987 , GRCh37.p13 chr4: 141,224,088-141,224,141 SCOC-AS1, SCOC
    nsv5894682copy number variation1nstd209human GRCh38 chr4: 140,321,619-140,326,128 , GRCh37.p13 chr4: 141,242,773-141,247,282 SCOC, SCOC-AS1
    nsv5892032copy number variation1nstd209human GRCh38 chr4: 140,287,108-140,287,445 , GRCh37.p13 chr4: 141,208,262-141,208,599 SCOC-AS1, SCOC
    nsv5837401copy number variation1nstd209human GRCh38 chr4: 140,321,583-140,326,082 , GRCh37.p13 chr4: 141,242,737-141,247,236 SCOC, SCOC-AS1
    nsv5623540insertion1nstd207human GRCh38 chr4: 140,362,273-140,362,273 , GRCh37.p13 chr4: 141,283,427-141,283,427 SCOC-AS1, SCOC
    nsv5611516insertion2nstd207human GRCh38 chr4: 140,362,299-140,362,299 , GRCh37.p13 chr4: 141,283,453-141,283,453 SCOC-AS1, SCOC
    nsv5577928copy number variation1nstd207human GRCh38 chr4: 140,302,934-140,302,987 , GRCh37.p13 chr4: 141,224,088-141,224,141 SCOC, SCOC-AS1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5552027insertion1nstd206human GRCh38 chr4: 140,353,398-140,353,447 , GRCh37.p13 chr4: 141,274,552-141,274,601 SCOC, SCOC-AS1
    nsv5470514copy number variation1nstd206human GRCh38 chr4: 140,321,622-140,326,129 , GRCh37.p13 chr4: 141,242,776-141,247,283 SCOC-AS1, SCOC
    nsv5469747copy number variation1nstd206human GRCh38 chr4: 140,378,672-140,378,773 , GRCh37.p13 chr4: 141,299,826-141,299,927 SCOC
    nsv5468228copy number variation1nstd206human GRCh38 chr4: 140,302,936-140,302,988 , GRCh37.p13 chr4: 141,224,090-141,224,142 SCOC-AS1, SCOC
    nsv5454507copy number variation1nstd206human GRCh38 chr4: 140,287,088-140,287,466 , GRCh37.p13 chr4: 141,208,242-141,208,620 SCOC-AS1, SCOC
    nsv5453921copy number variation1nstd206human GRCh38 chr4: 140,351,237-140,351,347 , GRCh37.p13 chr4: 141,272,391-141,272,501 SCOC-AS1, SCOC
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5320067copy number variation1nstd204human GRCh37.p13 chr4: 141,207,058-141,207,157 , GRCh38.p13 chr4: 140,285,904-140,286,003 SCOC, SCOC-AS1
    nsv5319465copy number variation1nstd204human GRCh37.p13 chr4: 141,213,775-141,215,780 , GRCh38.p13 chr4: 140,292,621-140,294,626 SCOC, SCOC-AS1
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