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Items: 1 to 20 of 348

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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
    nsv7076280inversion1nstd229human GRCh38 chr17: 18,608,940-18,821,521 , GRCh37.p13 chr17: 18,512,253-18,724,834 TRIM16L, LOC107985051, 8 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
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7063500inversion1nstd229human GRCh38 chr17: 18,620,305-18,830,721 , GRCh37.p13 chr17: 18,523,618-18,734,034 TBC1D28, PAIP1P2, 7 more genes
    nsv6985418copy number variation1nstd229human GRCh38 chr17: 18,680,268-18,683,699 , GRCh37.p13 chr17: 18,583,581-18,587,012 ZNF286B, FOXO3B
    nsv6985205copy number variation1nstd229human GRCh38 chr17: 18,667,606-18,672,392 , GRCh37.p13 chr17: 18,570,919-18,575,705 ZNF286B, FOXO3B
    nsv6981025copy number variation1nstd229human GRCh38 chr17: 18,669,682-18,670,193 , GRCh37.p13 chr17: 18,572,995-18,573,506 ZNF286B, FOXO3B
    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
    nsv6624204copy number variation1nstd224human GRCh37 chr17: 18,565,500-18,584,142 , GRCh38.p12 chr17: 18,662,187-18,680,829 FOXO3B, ZNF286B, 1 more genes
    nsv6624052copy number variation1nstd224human GRCh37 chr17: 18,541,626-18,923,818 , GRCh38.p12 chr17: 18,638,313-19,020,505 FOXO3B, PRPSAP2, 13 more genes
    nsv6624051copy number variation1nstd224human GRCh37 chr17: 18,408,965-18,923,818 , GRCh38.p12 chr17: 18,505,651-19,020,505 GRAP, SLC5A10, 19 more genes
    nsv6624017copy number variation1nstd224human GRCh37 chr17: 18,155,870-18,702,230 , GRCh38.p12 chr17: 18,252,556-18,798,917 SHMT1, SRP68P2, 33 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
    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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