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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7095341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,289,526-6,616,652 , GRCh38.p12 chr17: 5,386,206-6,713,333 RNA5SP435, DHX33, 31 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv6994424copy number variation1nstd229human GRCh38 chr17: 5,408,901-5,469,700 , GRCh37.p13 chr17: 5,312,221-5,373,020 RPAIN, DHX33-DT, 4 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6624289copy number variation1nstd224human GRCh37 chr17: 4,948,344-6,354,965 , GRCh38.p12 chr17: 5,045,049-6,451,645 C1QBP, NUP88, 32 more genes
    nsv6592364inversion1nstd223human GRCh38 chr17: 2,078,667-6,081,513 , GRCh37.p13 chr17: 1,981,961-5,984,833 MYBBP1A, CXCL16, 143 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 more genes
    nsv6133065copy number variation1nstd213human GRCh37 chr17: 4,530,000-8,270,001 , GRCh38.p12 chr17: 4,626,705-8,366,683 ACADVL, ALOX12, 206 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv5521849copy number variation1nstd206human GRCh38 chr17: 5,468,111-5,468,179 , GRCh37.p13 chr17: 5,371,431-5,371,499 DHX33-DT, DHX33
    nsv5297565copy number variation1nstd204human GRCh38.p13 chr17: 5,436,401-5,488,300 , GRCh37.p13 chr17: 5,339,721-5,391,620 DHX33, MIS12, 3 more genes
    nsv5031337inversion1nstd200human GRCh38 chr17: 5,462,212-6,246,469 , GRCh37.p13 chr17: 5,365,532-6,149,789 NLRP1, DHX33-DT, 12 more genes
    nsv5015650copy number variation1nstd200human GRCh38 chr17: 5,468,111-5,468,179 , GRCh37.p13 chr17: 5,371,431-5,371,499 DHX33, DHX33-DT
    nsv5015648copy number variation1nstd200human GRCh38 chr17: 5,452,804-5,467,823 , GRCh37.p13 chr17: 5,356,124-5,371,143 DHX33, DHX33-DT
    nsv4857861copy number variation1nstd200human GRCh37 chr17: 5,371,431-5,371,499 , GRCh38.p12 chr17: 5,468,111-5,468,179 DHX33-DT, DHX33
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729877copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,143,295-5,850,209 , GRCh38.p12 chr17: 5,240,000-5,946,889 DHX33, MIS12, 14 more genes
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