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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6728754copy number variation1nstd229human GRCh38 chr3: 163,391,544-165,609,812 , GRCh37.p13 chr3: 163,109,332-165,327,600 LINC02023, LOC107986050, 13 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6557256inversion1nstd223human GRCh38 chr3: 164,887,678-167,376,588 , GRCh37.p13 chr3: 164,605,466-167,094,376 PPIAP74, LOC105374194, 18 more genes
    nsv6360089copy number variation1nstd223human GRCh38 chr3: 165,184,101-165,185,100 , GRCh37.p13 chr3: 164,901,889-164,902,888 SLITRK3
    nsv6357508copy number variation1nstd223human GRCh38 chr3: 164,869,090-165,904,694 , GRCh37.p13 chr3: 164,586,878-165,622,482 BCHE, SI, 5 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5991951copy number variation1nstd212human GRCh38 chr3: 165,196,896-165,196,957 , GRCh37.p13 chr3: 164,914,684-164,914,745 SLITRK3
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5352132translocation1nstd200human GRCh38 chr3: 165,197,202-165,197,202 , GRCh38 chr3: 165,197,281-165,197,281 , GRCh37.p13 chr3: 164,915,069-164,915,069 , GRCh37.p13 chr3: 164,914,990-164,914,990 SLITRK3
    nsv5338174translocation1nstd200human GRCh37 chr3: 164,915,069-164,915,069 , GRCh37 chr3: 164,914,990-164,914,990 , GRCh38.p12 chr3: 165,197,202-165,197,202 , GRCh38.p12 chr3: 165,197,281-165,197,281 SLITRK3
    nsv5301964copy number variation1nstd204human GRCh38.p13 chr3: 165,042,891-165,201,199 , GRCh37.p13 chr3: 164,760,679-164,918,987 SI, LOC105374192, 2 more genes
    nsv5225119copy number variation1nstd204human GRCh38.p13 chr3: 165,042,901-165,201,200 , GRCh37.p13 chr3: 164,760,689-164,918,988 SLITRK3, LINC02023, 2 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924792copy number variation1nstd200human GRCh38 chr3: 165,042,899-165,201,197 , GRCh37.p13 chr3: 164,760,687-164,918,985 SLITRK3, LINC02023, 2 more genes
    nsv4804955copy number variation1nstd200human GRCh37 chr3: 164,760,687-164,918,985 , GRCh38.p12 chr3: 165,042,899-165,201,197 LINC02023, SI, 2 more genes
    nsv4587842copy number variation1nstd183human GRCh37 chr3: 164,880,233-164,935,804 , GRCh38.p12 chr3: 165,162,445-165,218,016 SLITRK3, LINC01322
    nsv4587683copy number variation1nstd183human GRCh37 chr3: 163,122,559-165,203,349 , GRCh38.p12 chr3: 163,404,771-165,485,561 MIR1263, LINC02023, 13 more genes
    nsv4566895sequence alteration1nstd166human GRCh37.p13 chr3: 164,902,770-164,905,302 , GRCh38.p12 chr3: 165,184,982-165,187,514 SLITRK3
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
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