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Items: 1 to 20 of 1097

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5980147insertion1nstd209human GRCh38 chr10: 131,095,232-131,095,232 , GRCh37.p13 chr10: 132,893,495-132,893,495 TCERG1L, TCERG1L-AS1
    nsv5972456insertion1nstd209human GRCh38 chr10: 131,176,845-131,176,845 , GRCh37.p13 chr10: 132,975,108-132,975,108 TCERG1L
    nsv5971348inversion1nstd209human GRCh38 chr10: 131,278,708-131,281,783 , GRCh37.p13 chr10: 133,076,971-133,080,046 TCERG1L
    nsv5926699copy number variation1nstd209human GRCh38 chr10: 131,246,921-131,247,008 , GRCh37.p13 chr10: 133,045,184-133,045,271 TCERG1L
    nsv5926625copy number variation1nstd209human GRCh38 chr10: 131,204,745-131,204,822 , GRCh37.p13 chr10: 133,003,008-133,003,085 TCERG1L, LOC105378563
    nsv5926414copy number variation1nstd209human GRCh38 chr10: 131,230,939-131,231,131 , GRCh37.p13 chr10: 133,029,202-133,029,394 TCERG1L
    nsv5925872copy number variation1nstd209human GRCh38 chr10: 131,289,597-131,289,713 , GRCh37.p13 chr10: 133,087,860-133,087,976 TCERG1L
    nsv5924508copy number variation1nstd209human GRCh38 chr10: 131,110,795-131,114,515 , GRCh37.p13 chr10: 132,909,058-132,912,778 TCERG1L
    nsv5923892copy number variation1nstd209human GRCh38 chr10: 131,209,344-131,209,409 , GRCh37.p13 chr10: 133,007,607-133,007,672 TCERG1L
    nsv5920783copy number variation1nstd209human GRCh38 chr10: 131,190,421-131,192,940 , GRCh37.p13 chr10: 132,988,684-132,991,203 TCERG1L
    nsv5917710copy number variation1nstd209human GRCh38 chr10: 131,300,757-131,305,916 , GRCh37.p13 chr10: 133,099,020-133,104,179 TCERG1L
    nsv5916944copy number variation1nstd209human GRCh38 chr10: 131,106,996-131,107,075 , GRCh37.p13 chr10: 132,905,259-132,905,338 TCERG1L
    nsv5915688copy number variation1nstd209human GRCh38 chr10: 131,049,156-131,126,884 , GRCh37.p13 chr10: 132,847,419-132,925,147 TCERG1L, TCERG1L-AS1, 1 more genes
    nsv5913113copy number variation1nstd209human GRCh38 chr10: 131,249,356-131,249,450 , GRCh37.p13 chr10: 133,047,619-133,047,713 TCERG1L
    nsv5912912copy number variation1nstd209human GRCh38 chr10: 131,126,505-131,126,566 , GRCh37.p13 chr10: 132,924,768-132,924,829 TCERG1L
    nsv5912752copy number variation1nstd209human GRCh38 chr10: 131,172,242-131,172,319 , GRCh37.p13 chr10: 132,970,505-132,970,582 TCERG1L
    nsv5911412copy number variation1nstd209human GRCh38 chr10: 131,108,402-131,108,464 , GRCh37.p13 chr10: 132,906,665-132,906,727 TCERG1L
    nsv5909990copy number variation1nstd209human GRCh38 chr10: 131,176,309-131,176,684 , GRCh37.p13 chr10: 132,974,572-132,974,947 TCERG1L
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