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Items: 1 to 20 of 692

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146253insertion1nstd232human GRCh37.p13 chr2: 167,169,518-167,169,518 , GRCh38.p12 chr2: 166,313,008-166,313,008 SCN9A
    nsv7145015copy number variation1nstd232human GRCh37.p13 chr2: 167,058,047-167,058,162 , GRCh38.p12 chr2: 166,201,537-166,201,652 SCN9A, SCN1A-AS1
    nsv7137058copy number variation1nstd102humanPathogenic GRCh37 chr2: 166,872,248-167,334,216 , GRCh38.p12 chr2: 166,015,738-166,477,706 SCN1A, SCN7A, 4 more genes
    nsv7096581copy number variation1nstd102humanUncertain significance GRCh37 chr2: 167,160,728-167,168,266 , GRCh38.p12 chr2: 166,304,218-166,311,756 SCN9A
    nsv7096579copy number variation2nstd102humanPathogenic GRCh37 chr2: 166,895,913-167,145,173 , GRCh38.p12 chr2: 166,039,403-166,288,663 RN7SKP152, SCN9A, 2 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
    nsv7096381copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 167,119,087-167,129,240 , GRCh38.p12 chr2: 166,262,577-166,272,730 SCN9A, SCN1A-AS1
    nsv7096379copy number variation1nstd102humanPathogenic GRCh37 chr2: 166,847,749-167,060,980 , GRCh38.p12 chr2: 165,991,239-166,204,470 RN7SKP152, SCN9A, 3 more genes
    nsv7096210copy number variation1nstd102humanUncertain significance GRCh37 chr2: 167,128,889-167,129,405 , GRCh38.p12 chr2: 166,272,379-166,272,895 SCN9A, SCN1A-AS1
    nsv7095869copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,085,181-167,168,266 , GRCh38.p12 chr2: 166,228,671-166,311,756 SCN9A, SCN1A-AS1
    nsv7095868copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,083,057-167,099,186 , GRCh38.p12 chr2: 166,226,547-166,242,676 SCN9A, SCN1A-AS1
    nsv7095867copy number variation1nstd102humanUncertain significance GRCh37 chr2: 167,055,182-167,143,153 , GRCh38.p12 chr2: 166,198,672-166,286,643 SCN9A, SCN1A-AS1
    nsv7095866copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,055,182-167,056,394 , GRCh38.p12 chr2: 166,198,672-166,199,884 SCN1A-AS1, SCN9A
    nsv7054462inversion1nstd229human GRCh38 chr2: 166,194,329-166,194,702 , GRCh37.p13 chr2: 167,050,839-167,051,212 SCN9A, SCN1A-AS1
    nsv6697625copy number variation1nstd229human GRCh38 chr2: 166,186,245-166,195,984 , GRCh37.p13 chr2: 167,042,755-167,052,494 SCN9A, SCN1A-AS1
    nsv6695920copy number variation1nstd229human GRCh38 chr2: 166,369,502-166,369,533 , GRCh37.p13 chr2: 167,226,012-167,226,043 SCN9A
    nsv6695471copy number variation1nstd229human GRCh38 chr2: 166,191,608-166,197,220 , GRCh37.p13 chr2: 167,048,118-167,053,730 SCN9A, SCN1A-AS1
    nsv6692502copy number variation1nstd229human GRCh38 chr2: 166,302,201-166,307,900 , GRCh37.p13 chr2: 167,158,711-167,164,410 SCN1A-AS1, SCN9A
    nsv6691819copy number variation1nstd229human GRCh38 chr2: 166,299,171-166,302,286 , GRCh37.p13 chr2: 167,155,681-167,158,796 SCN9A, SCN1A-AS1
    nsv6690395copy number variation1nstd229human GRCh38 chr2: 166,240,092-166,334,623 , GRCh37.p13 chr2: 167,096,602-167,191,133 SCN9A, SCN1A-AS1
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