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Items: 1 to 20 of 1267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7147636insertion1nstd232human GRCh37.p13 chr8: 143,323,604-143,323,604 , GRCh38.p12 chr8: 142,242,243-142,242,243 TSNARE1
    nsv7146094copy number variation1nstd232human GRCh37.p13 chr8: 143,439,580-143,439,638 , GRCh38.p12 chr8: 142,358,219-142,358,277 TSNARE1
    nsv7144906insertion1nstd232human GRCh37.p13 chr8: 143,304,553-143,304,553 , GRCh38.p12 chr8: 142,223,192-142,223,192 TSNARE1
    nsv7143779copy number variation1nstd232human GRCh37.p13 chr8: 143,471,977-143,472,038 , GRCh38.p12 chr8: 142,390,616-142,390,677 TSNARE1
    nsv7141843copy number variation1nstd232human GRCh37.p13 chr8: 143,431,503-143,431,553 , GRCh38.p12 chr8: 142,350,142-142,350,192 TSNARE1
    nsv7140954insertion1nstd232human GRCh37.p13 chr8: 143,435,217-143,435,217 , GRCh38.p12 chr8: 142,353,856-142,353,856 TSNARE1
    nsv7140487insertion1nstd232human GRCh37.p13 chr8: 143,304,554-143,304,554 , GRCh38.p12 chr8: 142,223,193-142,223,193 TSNARE1
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7063396inversion1nstd229human GRCh38 chr8: 142,372,234-142,404,121 , GRCh37.p13 chr8: 143,453,595-143,485,482 TSNARE1
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv7060830inversion1nstd229human GRCh38 chr8: 142,327,331-142,403,731 , GRCh37.p13 chr8: 143,408,692-143,485,092 TSNARE1
    nsv7058897inversion1nstd229human GRCh38 chr8: 142,345,706-142,345,832 , GRCh37.p13 chr8: 143,427,067-143,427,193 TSNARE1
    nsv6877863copy number variation1nstd229human GRCh38 chr8: 142,316,691-142,317,180 , GRCh37.p13 chr8: 143,398,052-143,398,541 TSNARE1
    nsv6877827copy number variation1nstd229human GRCh38 chr8: 142,327,318-142,335,944 , GRCh37.p13 chr8: 143,408,679-143,417,305 TSNARE1
    nsv6877621copy number variation1nstd229human GRCh38 chr8: 142,220,451-142,234,322 , GRCh37.p13 chr8: 143,301,812-143,315,683 TSNARE1
    nsv6877567copy number variation1nstd229human GRCh38 chr8: 142,096,201-142,296,000 , GRCh37.p13 chr8: 143,177,562-143,377,361 LINC00051, RN7SL260P, 3 more genes
    nsv6877436copy number variation1nstd229human GRCh38 chr8: 142,336,931-142,355,162 , GRCh37.p13 chr8: 143,418,292-143,436,523 TSNARE1
    nsv6875887copy number variation1nstd229human GRCh38 chr8: 142,258,235-142,349,581 , GRCh37.p13 chr8: 143,339,596-143,430,942 TSNARE1
    nsv6875611copy number variation1nstd229human GRCh38 chr8: 142,272,145-142,272,689 , GRCh37.p13 chr8: 143,353,506-143,354,050 TSNARE1
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