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Items: 1 to 20 of 148

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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
    nsv7094906copy number variation1nstd102humanPathogenic GRCh37 chr17: 5,336,335-5,337,107 , GRCh38.p12 chr17: 5,433,015-5,433,787 RPAIN, C1QBP
    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
    nsv6992809copy number variation1nstd229human GRCh38 chr17: 5,425,601-5,431,200 , GRCh37.p13 chr17: 5,328,921-5,334,520 RPAIN, C1QBP
    nsv6984560copy number variation1nstd229human GRCh38 chr17: 5,435,303-5,439,658 , GRCh37.p13 chr17: 5,338,623-5,342,978 DHX33, C1QBP
    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
    nsv6981886copy number variation1nstd229human GRCh38 chr17: 5,432,619-5,433,445 , GRCh37.p13 chr17: 5,335,939-5,336,765 C1QBP, RPAIN
    nsv6978495copy number variation1nstd229human GRCh38 chr17: 5,429,921-5,435,918 , GRCh37.p13 chr17: 5,333,241-5,339,238 C1QBP, RPAIN
    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
    nsv6513228copy number variation1nstd223human GRCh38 chr17: 5,435,632-5,436,749 , GRCh37.p13 chr17: 5,338,952-5,340,069 C1QBP
    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
    nsv6031979copy number variation1nstd212human GRCh38 chr17: 5,431,224-5,431,358 , GRCh37.p13 chr17: 5,334,544-5,334,678 RPAIN, C1QBP
    nsv5938068copy number variation1nstd209human GRCh38 chr17: 5,435,768-5,436,757 , GRCh37.p13 chr17: 5,339,088-5,340,077 C1QBP
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