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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6985680copy number variation1nstd229human GRCh38 chr17: 50,775,414-50,839,566 , GRCh37.p13 chr17: 48,852,775-48,916,927 WFIKKN2
    nsv6985415copy number variation1nstd229human GRCh38 chr17: 50,743,521-50,877,038 , GRCh37.p13 chr17: 48,820,882-48,954,399 TOB1-AS1, RPL5P33, 5 more genes
    nsv6984145copy number variation1nstd229human GRCh38 chr17: 50,842,571-50,850,627 , GRCh37.p13 chr17: 48,919,932-48,927,988 RPL5P33, WFIKKN2
    nsv6983143copy number variation1nstd229human GRCh38 chr17: 50,751,981-50,835,460 , GRCh37.p13 chr17: 48,829,342-48,912,821 MIR8059, LUC7L3, 2 more genes
    nsv6133358copy number variation1nstd213human GRCh37 chr17: 48,890,000-49,210,001 , GRCh38.p12 chr17: 50,812,639-51,132,640 SPAG9, TOB1, 4 more genes
    nsv6039772copy number variation1nstd212human GRCh38 chr17: 50,836,524-50,836,606 , GRCh37.p13 chr17: 48,913,885-48,913,967 WFIKKN2
    nsv5587754copy number variation1nstd207human GRCh38 chr17: 50,836,475-50,836,591 , GRCh37.p13 chr17: 48,913,836-48,913,952 WFIKKN2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5159340mobile element insertion1nstd203human GRCh38 chr17: 50,839,152-50,839,156 , GRCh37.p13 chr17: 48,916,513-48,916,517 WFIKKN2
    nsv4867265copy number variation1nstd200human GRCh37 chr17: 48,910,313-48,910,518 , GRCh38.p12 chr17: 50,832,952-50,833,157 WFIKKN2
    nsv4734284copy number variation1nstd199human GRCh37 chr17: 48,913,874-48,913,990 , GRCh38.p12 chr17: 50,836,513-50,836,629 WFIKKN2
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3912763copy number variation1nstd102humanPathogenic NCBI36 chr17: 44,570,225-47,580,169 , GRCh37 chr17: 47,215,226-50,225,170 , GRCh38 chr17: 49,137,864-52,147,810 CACNA1G, SUMO2P7, 77 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
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