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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5528228copy number variation1nstd206human GRCh38 chr17: 19,294,537-19,295,691 , GRCh37.p13 chr17: 19,197,850-19,199,004 EPN2-AS1, EPN2
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5381797copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,145,361-20,137,943 , GRCh38.p12 chr17: 17,242,047-20,234,630 LOC644909, FLII, 117 more genes
    nsv5295477copy number variation1nstd204human GRCh38.p13 chr17: 19,060,401-19,303,300 , GRCh37.p13 chr17: 18,963,714-19,206,613 GRAPL, EPN2-AS1, 13 more genes
    nsv4858293copy number variation1nstd200human GRCh37 chr17: 19,197,984-19,198,952 , GRCh38.p12 chr17: 19,294,671-19,295,639 EPN2-AS1, EPN2
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729895copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,746,987-20,231,379 , GRCh38.p12 chr17: 18,843,674-20,328,066 NDUFB4P3, SNORD3A, 52 more genes
    nsv4729886copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,763,370-20,395,611 , GRCh38.p12 chr17: 16,860,056-20,492,298 LOC100419620, PAIP1P2, 139 more genes
    nsv4729810copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,761,814-20,330,062 , GRCh38.p12 chr17: 16,858,500-20,426,749 PRPSAP2, EPN2, 134 more genes
    nsv4624188copy number variation1nstd183human GRCh37 chr17: 19,145,948-19,352,628 , GRCh38.p12 chr17: 19,242,635-19,449,315 B9D1, EPN2-AS1, 10 more genes
    nsv4531970copy number variation1nstd166human GRCh37.p13 chr17: 19,134,897-19,205,000 , GRCh38.p12 chr17: 19,231,584-19,301,687 EPN2-AS1, EPN2, 1 more genes
    nsv4531617copy number variation1nstd166human GRCh37.p13 chr17: 19,199,752-19,201,439 , GRCh38.p12 chr17: 19,296,439-19,298,126 EPN2, EPN2-AS1
    nsv4349342copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,842,991-20,217,316 , GRCh38.p12 chr17: 16,939,677-20,314,003 LOC105371566, LOC105371569, 126 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4250196copy number variation1nstd166human GRCh37.p13 chr17: 19,208,770-19,208,829 , GRCh38.p12 chr17: 19,305,457-19,305,516 EPN2-AS1, EPN2
    nsv4238132copy number variation1nstd166human GRCh37.p13 chr17: 19,208,115-19,208,171 , GRCh38.p12 chr17: 19,304,802-19,304,858 EPN2-AS1, EPN2
    nsv4235211copy number variation1nstd166human GRCh37.p13 chr17: 19,152,063-19,442,203 , GRCh38.p12 chr17: 19,248,750-19,538,890 , EPN2-AS1, 14 more genes
    nsv3965365inversion1nstd168human GRCh38 chr17: 18,448,724-20,345,591 , GRCh37.p13 chr17: 18,352,038-20,248,904 , ALDH3A1, 76 more genes
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