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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099192copy number variation1nstd231human GRCh38.p12 chr1: 31,395,299-32,087,194 , GRCh37 chr1: 31,868,146-32,552,795 ADGRB2, COL16A1, 19 more genes
    nsv7046389inversion1nstd229human GRCh38 chr1: 31,492,639-36,569,102 , GRCh37.p13 chr1: 32,017,064-37,034,703 LOC105378642, TMEM35B, 127 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648886copy number variation1nstd229human GRCh38 chr1: 32,096,676-32,096,715 , GRCh37.p13 chr1: 32,562,277-32,562,316 TMEM39B
    nsv6648884copy number variation1nstd229human GRCh38 chr1: 32,080,032-32,084,844 , GRCh37.p13 chr1: 32,545,633-32,550,445 TMEM39B
    nsv6648743copy number variation1nstd229human GRCh38 chr1: 32,076,958-32,091,523 , GRCh37.p13 chr1: 32,542,559-32,557,124 MIR5585, TMEM39B
    nsv6648694copy number variation1nstd229human GRCh38 chr1: 32,078,875-32,082,959 , GRCh37.p13 chr1: 32,544,476-32,548,560 TMEM39B
    nsv6648244copy number variation1nstd229human GRCh38 chr1: 32,085,563-32,087,433 , GRCh37.p13 chr1: 32,551,164-32,553,034 TMEM39B, MIR5585
    nsv6648243copy number variation1nstd229human GRCh38 chr1: 32,082,501-32,085,800 , GRCh37.p13 chr1: 32,548,102-32,551,401 TMEM39B, MIR5585
    nsv6648242copy number variation1nstd229human GRCh38 chr1: 32,078,801-32,084,100 , GRCh37.p13 chr1: 32,544,402-32,549,701 TMEM39B
    nsv6648241copy number variation1nstd229human GRCh38 chr1: 32,070,397-32,072,005 , GRCh37.p13 chr1: 32,535,998-32,537,606 TMEM39B
    nsv6648240copy number variation1nstd229human GRCh38 chr1: 32,069,307-32,093,212 , GRCh37.p13 chr1: 32,534,908-32,558,813 MIR5585, TMEM39B
    nsv6547695inversion1nstd223human GRCh38 chr1: 32,097,709-32,098,711 , GRCh37.p13 chr1: 32,563,310-32,564,312 TMEM39B
    nsv6536539inversion1nstd223human GRCh38 chr1: 32,079,796-32,080,597 , GRCh37.p13 chr1: 32,545,397-32,546,198 TMEM39B
    nsv6333680copy number variation1nstd223human GRCh38 chr1: 32,087,792-32,097,865 , GRCh37.p13 chr1: 32,553,393-32,563,466 TMEM39B
    nsv6333110copy number variation1nstd223human GRCh38 chr1: 32,085,559-32,087,351 , GRCh37.p13 chr1: 32,551,160-32,552,952 TMEM39B, MIR5585
    nsv6327360copy number variation1nstd223human GRCh38 chr1: 32,083,677-32,084,821 , GRCh37.p13 chr1: 32,549,278-32,550,422 TMEM39B
    nsv6325202copy number variation1nstd223human GRCh38 chr1: 32,078,801-32,081,900 , GRCh37.p13 chr1: 32,544,402-32,547,501 TMEM39B
    nsv6319554copy number variation1nstd223human GRCh38 chr1: 32,079,857-32,107,225 , GRCh37.p13 chr1: 32,545,458-32,572,826 KPNA6, TMEM39B, 1 more genes
    nsv6318473copy number variation1nstd223human GRCh38 chr1: 32,088,882-32,090,707 , GRCh37.p13 chr1: 32,554,483-32,556,308 TMEM39B
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