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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7065329inversion1nstd229human GRCh38 chr17: 75,958,231-76,360,906 , GRCh37.p13 chr17: 73,954,312-74,356,987 RNF157, ACOX1, 20 more genes
    nsv6996898copy number variation1nstd229human GRCh38 chr17: 76,073,965-76,081,615 , GRCh37.p13 chr17: 74,070,046-74,077,696 GALR2, EXOC7, 1 more genes
    nsv6994761copy number variation1nstd229human GRCh38 chr17: 76,095,384-76,097,512 , GRCh37.p13 chr17: 74,091,465-74,093,593 MIR6868, EXOC7
    nsv6988360copy number variation1nstd229human GRCh38 chr17: 76,100,366-76,114,622 , GRCh37.p13 chr17: 74,096,447-74,110,703 EXOC7
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6979368copy number variation1nstd229human GRCh38 chr17: 76,096,074-76,096,244 , GRCh37.p13 chr17: 74,092,155-74,092,325 MIR6868, EXOC7
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6577785inversion1nstd223human GRCh38 chr17: 76,096,233-76,096,822 , GRCh37.p13 chr17: 74,092,314-74,092,903 MIR6868, EXOC7
    nsv6529508copy number variation1nstd223human GRCh38 chr17: 76,095,384-76,097,506 , GRCh37.p13 chr17: 74,091,465-74,093,587 EXOC7, MIR6868
    nsv6527035copy number variation1nstd223human GRCh38 chr17: 76,098,632-76,098,935 , GRCh37.p13 chr17: 74,094,713-74,095,016 EXOC7
    nsv6517791copy number variation1nstd223human GRCh38 chr17: 76,100,162-76,100,935 , GRCh37.p13 chr17: 74,096,243-74,097,016 EXOC7
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6038748copy number variation1nstd212human GRCh38 chr17: 76,098,295-76,098,389 , GRCh37.p13 chr17: 74,094,376-74,094,470 MIR6868, EXOC7
    nsv5932819copy number variation1nstd209human GRCh38 chr17: 76,082,936-76,082,991 , GRCh37.p13 chr17: 74,079,017-74,079,072 EXOC7, ZACN
    nsv5883020copy number variation1nstd209human GRCh38 chr17: 76,095,027-76,097,326 , GRCh37.p13 chr17: 74,091,108-74,093,407 EXOC7, MIR6868
    nsv5518558copy number variation1nstd206human GRCh38 chr17: 76,100,162-76,100,935 , GRCh37.p13 chr17: 74,096,243-74,097,016 EXOC7
    nsv5515588copy number variation1nstd206human GRCh38 chr17: 76,098,358-76,110,794 , GRCh37.p13 chr17: 74,094,439-74,106,875 MIR6868, EXOC7
    nsv5365792translocation1nstd200human GRCh38 chr17: 76,097,512-76,097,512 , GRCh38 chr17: 76,095,384-76,095,384 , GRCh37.p13 chr17: 74,093,593-74,093,593 , GRCh37.p13 chr17: 74,091,465-74,091,465 EXOC7, MIR6868
    nsv5349673translocation1nstd200human GRCh38 chr17: 76,097,473-76,097,473 , GRCh38 chr17: 76,097,609-76,097,609 , GRCh37.p13 chr17: 74,093,554-74,093,554 , GRCh37.p13 chr17: 74,093,690-74,093,690 EXOC7, MIR6868
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