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Items: 1 to 20 of 389

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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
    nsv7143596copy number variation1nstd232human GRCh37.p13 chr17: 1,373,627-1,373,726 , GRCh38.p12 chr17: 1,470,333-1,470,432 MYO1C
    nsv7142262copy number variation1nstd232human GRCh37.p13 chr17: 1,383,918-1,383,997 , GRCh38.p12 chr17: 1,480,624-1,480,703 MYO1C
    nsv7098743copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-2,585,096 , GRCh38.p12 chr17: 519,128-2,681,802 PAFAH1B1, RN7SL33P, 65 more genes
    nsv7098729copy number variation1nstd102humanPathogenic GRCh37 chr17: 422,368-1,945,151 , GRCh38.p12 chr17: 519,128-2,041,857 MYO1C, SERPINF1, 42 more genes
    nsv7094928copy number variation1nstd102humanPathogenic GRCh37 chr17: 882,539-1,387,567 , GRCh38.p12 chr17: 979,299-1,484,273 , GRCh38.p12 chr17|NT_187613.1: 18,546-391,357 MIR3183, ABR, 11 more genes
    nsv7094896copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-1,680,740 , GRCh38.p12 chr17: 519,128-1,777,446 SLC43A2, LOC105371480, 34 more genes
    nsv7077625inversion1nstd229human GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981 MIR3183, YWHAE, 75 more genes
    nsv7075634inversion1nstd229human GRCh38 chr17: 1,370,296-2,529,284 , GRCh37.p13 chr17: 1,273,590-2,432,578 MCUR1P1, CRK, 42 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
    nsv7072232inversion1nstd229human GRCh38 chr17: 1,370,504-2,529,584 , GRCh37.p13 chr17: 1,273,798-2,432,878 MNT, SMG6, 42 more genes
    nsv6991290copy number variation1nstd229human GRCh38 chr17: 1,343,701-1,599,700 , GRCh37.p13 chr17: 1,246,995-1,502,994 INPP5K, PITPNA, 6 more genes
    nsv6987892copy number variation1nstd229human GRCh38 chr17: 1,469,089-1,469,370 , GRCh37.p13 chr17: 1,372,383-1,372,664 MYO1C
    nsv6981428copy number variation1nstd229human GRCh38 chr17: 1,467,201-1,472,200 , GRCh37.p13 chr17: 1,370,495-1,375,494 MYO1C
    nsv6981210copy number variation1nstd229human GRCh38 chr17: 1,461,472-1,486,481 , GRCh37.p13 chr17: 1,364,766-1,389,775 MYO1C
    nsv6979713copy number variation1nstd229human GRCh38 chr17: 1,472,806-1,472,920 , GRCh37.p13 chr17: 1,376,100-1,376,214 MYO1C
    nsv6637505copy number variation1nstd102humanPathogenic GRCh37 chr17: 526-1,690,452 , GRCh38.p12 chr17: 150,733-1,787,158 RPS4XP17, LIAT1, 43 more genes
    nsv6637325copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,095,592-3,484,368 , GRCh38.p12 chr17: 1,192,298-3,581,074 SLC43A2, LOC105371592, 81 more genes
    nsv6637292copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,377,247-2,455,613 , GRCh38.p12 chr17: 1,473,953-2,552,319 RPA1, TLCD2, 40 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
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