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Items: 1 to 20 of 546

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096575copy number variation1nstd102humanUncertain significance GRCh37 chr2: 166,018,798-166,246,334 , GRCh38.p12 chr2: 165,162,288-165,389,824 SCN2A, MAPRE1P3, 1 more genes
    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
    nsv7096374copy number variation1nstd102humanUncertain significance GRCh37 chr2: 165,984,121-166,246,334 , GRCh38.p12 chr2: 165,127,611-165,389,824 MAPRE1P3, SCN3A, 1 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
    nsv7044722inversion1nstd229human GRCh38 chr2: 165,165,367-165,165,395 , GRCh37.p13 chr2: 166,021,877-166,021,905 SCN3A
    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
    nsv6695611copy number variation1nstd229human GRCh38 chr2: 165,150,715-165,153,982 , GRCh37.p13 chr2: 166,007,225-166,010,492 SCN3A
    nsv6690030copy number variation1nstd229human GRCh38 chr2: 165,125,219-165,125,945 , GRCh37.p13 chr2: 165,981,729-165,982,455 SCN3A
    nsv6689857copy number variation1nstd229human GRCh38 chr2: 165,104,201-165,108,000 , GRCh37.p13 chr2: 165,960,711-165,964,510 SCN3A
    nsv6688573copy number variation1nstd229human GRCh38 chr2: 165,148,635-165,148,770 , GRCh37.p13 chr2: 166,005,145-166,005,280 SCN3A
    nsv6685689copy number variation1nstd229human GRCh38 chr2: 165,087,375-165,114,348 , GRCh37.p13 chr2: 165,943,885-165,970,858 SCN3A
    nsv6684152copy number variation1nstd229human GRCh38 chr2: 165,081,568-165,104,498 , GRCh37.p13 chr2: 165,938,078-165,961,008 SCN3A
    nsv6627776copy number variation1nstd224human GRCh37 chr2: 165,765,194-165,991,766 , GRCh38.p12 chr2: 164,908,684-165,135,256 SLC38A11, SCN3A
    nsv6544812inversion1nstd223human GRCh38 chr2: 165,156,216-165,156,905 , GRCh37.p13 chr2: 166,012,726-166,013,415 SCN3A
    nsv6541121inversion1nstd223human GRCh38 chr2: 165,159,681-165,159,889 , GRCh37.p13 chr2: 166,016,191-166,016,399 SCN3A
    nsv6352051copy number variation1nstd223human GRCh38 chr2: 165,202,701-165,203,800 , GRCh37.p13 chr2: 166,059,211-166,060,310 SCN3A
    nsv6345585copy number variation1nstd223human GRCh38 chr2: 165,129,794-165,130,191 , GRCh37.p13 chr2: 165,986,304-165,986,701 SCN3A
    nsv6341268copy number variation1nstd223human GRCh38 chr2: 165,170,201-165,170,900 , GRCh37.p13 chr2: 166,026,711-166,027,410 SCN3A
    nsv6340990copy number variation1nstd223human GRCh38 chr2: 165,104,180-165,107,946 , GRCh37.p13 chr2: 165,960,690-165,964,456 SCN3A
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