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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7061962inversion1nstd229human GRCh38 chr10: 61,552,058-61,719,657 , GRCh37.p13 chr10: 63,311,816-63,479,415 CABCOCO1
    nsv6896853copy number variation1nstd229human GRCh38 chr10: 61,727,261-61,731,011 , GRCh37.p13 chr10: 63,487,019-63,490,769 CABCOCO1
    nsv6896460copy number variation1nstd229human GRCh38 chr10: 61,655,554-61,662,122 , GRCh37.p13 chr10: 63,415,312-63,421,880 CABCOCO1
    nsv6895800copy number variation1nstd229human GRCh38 chr10: 61,661,690-61,711,489 , GRCh37.p13 chr10: 63,421,448-63,471,247 CABCOCO1
    nsv6895779copy number variation1nstd229human GRCh38 chr10: 61,717,427-61,717,462 , GRCh37.p13 chr10: 63,477,185-63,477,220 CABCOCO1
    nsv6895618copy number variation1nstd229human GRCh38 chr10: 61,698,501-61,709,000 , GRCh37.p13 chr10: 63,458,259-63,468,758 CABCOCO1
    nsv6892038copy number variation1nstd229human GRCh38 chr10: 61,690,801-61,697,800 , GRCh37.p13 chr10: 63,450,559-63,457,558 CABCOCO1
    nsv6887358copy number variation1nstd229human GRCh38 chr10: 61,673,683-61,695,173 , GRCh37.p13 chr10: 63,433,441-63,454,931 CABCOCO1
    nsv6886815copy number variation1nstd229human GRCh38 chr10: 61,757,463-61,783,055 , GRCh37.p13 chr10: 63,517,221-63,542,813 CABCOCO1, LINC02625
    nsv6884001copy number variation1nstd229human GRCh38 chr10: 57,418,641-61,973,578 , GRCh37.p13 chr10: 59,178,401-63,733,337 LINC02625, ARID5B, 40 more genes
    nsv6879686copy number variation1nstd229human GRCh38 chr10: 61,680,998-61,714,085 , GRCh37.p13 chr10: 63,440,756-63,473,843 CABCOCO1
    nsv6637363copy number variation1nstd102humanUncertain significance GRCh37 chr10: 57,941,252-64,846,332 , GRCh38.p12 chr10: 56,181,491-63,086,572 TMEM26-AS1, LOC112268068, 53 more genes
    nsv6637322copy number variation1nstd102humanUncertain significance GRCh37 chr10: 60,870,153-63,790,451 , GRCh38.p12 chr10: 59,110,393-62,030,692 MRPL50P4, CCDC6, 25 more genes
    nsv6620648copy number variation1nstd224human GRCh37 chr10: 63,415,264-63,601,824 , GRCh38.p12 chr10: 61,655,506-61,842,065 CABCOCO1, LINC02625
    nsv6454485copy number variation1nstd223human GRCh38 chr10: 61,732,101-61,733,400 , GRCh37.p13 chr10: 63,491,859-63,493,158 CABCOCO1
    nsv6451638copy number variation1nstd223human GRCh38 chr10: 61,697,101-61,697,900 , GRCh37.p13 chr10: 63,456,859-63,457,658 CABCOCO1
    nsv6451262copy number variation1nstd223human GRCh38 chr10: 61,661,901-61,666,000 , GRCh37.p13 chr10: 63,421,659-63,425,758 CABCOCO1
    nsv6451068copy number variation1nstd223human GRCh38 chr10: 61,666,501-61,668,200 , GRCh37.p13 chr10: 63,426,259-63,427,958 CABCOCO1
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