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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096574copy number variation1nstd102humanPathogenic GRCh37 chr2: 165,946,660-167,108,415 , GRCh38.p12 chr2: 165,090,150-166,251,905 SCN3A, MAPRE1P3, 11 more genes
    nsv7096373copy number variation1nstd102humanUncertain significance GRCh37 chr2: 165,946,660-166,894,662 , GRCh38.p12 chr2: 165,090,150-166,038,152 TTC21B, SCN3A, 8 more genes
    nsv7052305inversion1nstd229human GRCh38 chr2: 165,688,366-165,692,569 , GRCh37.p13 chr2: 166,544,876-166,549,079 CSRNP3
    nsv7046873inversion1nstd229human GRCh38 chr2: 165,549,110-165,579,094 , GRCh37.p13 chr2: 166,405,620-166,435,604 CSRNP3
    nsv7045029inversion1nstd229human GRCh38 chr2: 165,567,745-165,572,262 , GRCh37.p13 chr2: 166,424,255-166,428,772 CSRNP3
    nsv7044791inversion1nstd229human GRCh38 chr2: 165,530,435-165,530,457 , GRCh37.p13 chr2: 166,386,945-166,386,967 CSRNP3
    nsv7041761inversion1nstd229human GRCh38 chr2: 161,208,254-165,696,625 , GRCh37.p13 chr2: 162,064,765-166,553,135 SCN3A, LOC101929532, 45 more genes
    nsv7039552inversion1nstd229human GRCh38 chr2: 161,275,467-165,696,611 , GRCh37.p13 chr2: 162,131,978-166,553,121 LOC105373722, EIF3EP3, 42 more genes
    nsv6697918copy number variation1nstd229human GRCh38 chr2: 165,612,788-165,617,785 , GRCh37.p13 chr2: 166,469,298-166,474,295 CSRNP3
    nsv6697550copy number variation1nstd229human GRCh38 chr2: 165,633,501-165,635,600 , GRCh37.p13 chr2: 166,490,011-166,492,110 CSRNP3
    nsv6696473copy number variation1nstd229human GRCh38 chr2: 165,580,708-165,755,471 , GRCh37.p13 chr2: 166,437,218-166,611,981 CSRNP3, GALNT3
    nsv6693214copy number variation1nstd229human GRCh38 chr2: 165,611,301-165,617,300 , GRCh37.p13 chr2: 166,467,811-166,473,810 CSRNP3
    nsv6693133copy number variation1nstd229human GRCh38 chr2: 165,576,101-165,612,100 , GRCh37.p13 chr2: 166,432,611-166,468,610 CSRNP3
    nsv6691096copy number variation1nstd229human GRCh38 chr2: 165,475,029-165,538,924 , GRCh37.p13 chr2: 166,331,539-166,395,434 CSRNP3
    nsv6690931copy number variation1nstd229human GRCh38 chr2: 165,598,645-165,598,773 , GRCh37.p13 chr2: 166,455,155-166,455,283 CSRNP3
    nsv6690237copy number variation1nstd229human GRCh38 chr2: 165,658,194-165,658,257 , GRCh37.p13 chr2: 166,514,704-166,514,767 CSRNP3
    nsv6689931copy number variation1nstd229human GRCh38 chr2: 165,623,331-165,627,517 , GRCh37.p13 chr2: 166,479,841-166,484,027 CSRNP3
    nsv6688326copy number variation1nstd229human GRCh38 chr2: 165,594,701-165,604,900 , GRCh37.p13 chr2: 166,451,211-166,461,410 CSRNP3
    nsv6687589copy number variation1nstd229human GRCh38 chr2: 165,577,452-165,577,631 , GRCh37.p13 chr2: 166,433,962-166,434,141 CSRNP3
    nsv6687350copy number variation1nstd229human GRCh38 chr2: 165,683,437-165,725,610 , GRCh37.p13 chr2: 166,539,947-166,582,120 CSRNP3
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