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Items: 1 to 20 of 394

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137103copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,664,739-20,370,783 , GRCh38.p12 chr17: 16,761,425-20,467,470 NMTRQ-TTG12-1, NOS2P4, 148 more genes
    nsv7098881copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,116,969-20,217,378 , GRCh38.p12 chr17: 17,213,655-20,314,065 LOC105371578, SNORD3B-2, 119 more genes
    nsv7077532inversion1nstd229human GRCh38 chr17: 17,907,928-18,966,216 , GRCh37.p13 chr17: 17,811,242-18,869,529 SMCR8, PAIP1P2, 51 more genes
    nsv7073486inversion1nstd229human GRCh38 chr17: 15,622,817-18,740,940 , GRCh37.p13 chr17: 15,526,131-18,644,253 NCOR1, KRT16P6, 129 more genes
    nsv7073439inversion1nstd229human GRCh38 chr17: 15,962,151-19,146,977 , GRCh37.p13 chr17: 15,865,465-19,050,290 RNU6-767P, KRT17P5, 129 more genes
    nsv7073152inversion1nstd229human GRCh38 chr17: 17,317,750-18,724,343 , GRCh37.p13 chr17: 17,221,064-18,627,656 TOP3A, SMCR8, 60 more genes
    nsv7068050inversion1nstd229human GRCh38 chr17: 16,799,901-18,286,035 , GRCh37.p13 chr17: 16,703,215-18,189,349 ATPAF2, TNFRSF13B, 51 more genes
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7059177inversion1nstd229human GRCh38 chr17: 15,493,473-18,338,296 , GRCh37.p13 chr17: 15,396,787-18,241,610 TOM1L2, PPIAP53, 107 more genes
    nsv6998073copy number variation1nstd229human GRCh38 chr17: 17,954,562-17,971,900 , GRCh37.p13 chr17: 17,857,876-17,875,214 DRC3, TOM1L2
    nsv6995085copy number variation1nstd229human GRCh38 chr17: 17,971,446-17,986,952 , GRCh37.p13 chr17: 17,874,760-17,890,266 LOC107984989, TOM1L2, 2 more genes
    nsv6990375copy number variation1nstd229human GRCh38 chr17: 17,938,998-17,989,187 , GRCh37.p13 chr17: 17,842,312-17,892,501 BRI3P3, DRC3, 2 more genes
    nsv6989174copy number variation1nstd229human GRCh38 chr17: 17,997,789-18,010,573 , GRCh37.p13 chr17: 17,901,103-17,913,887 LOC100419436, DRC3
    nsv6988676copy number variation1nstd229human GRCh38 chr17: 17,993,726-17,993,808 , GRCh37.p13 chr17: 17,897,040-17,897,122 DRC3
    nsv6980953copy number variation1nstd229human GRCh38 chr17: 18,002,291-18,005,948 , GRCh37.p13 chr17: 17,905,605-17,909,262 DRC3
    nsv6637220copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,103,571-19,331,028 , GRCh38.p12 chr17: 17,200,257-19,427,715 PRPSAP2, SNORD3A, 96 more genes
    nsv6634447copy number variation1nstd102humanUncertain significance GRCh37 chr17: 16,736,709-20,339,460 , GRCh38.p12 chr17: 16,833,395-20,436,147 KCTD9P1, MTCO1P39, 139 more genes
    nsv6593366inversion1nstd223human GRCh38 chr17: 15,604,136-18,759,631 , GRCh37.p13 chr17: 15,507,450-18,662,944 EEF1A1P43, ZNF624, 131 more genes
    nsv6590468inversion1nstd223human GRCh38 chr17: 15,738,295-18,638,514 , GRCh37.p13 chr17: 15,641,609-18,541,827 LOC105371570, RAI1-AS1, 120 more genes
    nsv6587833inversion1nstd223human GRCh38 chr17: 15,680,260-18,702,090 , GRCh37.p13 chr17: 15,583,574-18,605,403 RPLP1P11, KRT16P6, 128 more genes
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