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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138715insertion1nstd232human GRCh37.p13 chr17: 48,778,077-48,778,077 , GRCh38.p12 chr17: 50,700,716-50,700,716 ANKRD40
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6995973copy number variation1nstd229human GRCh38 chr17: 50,705,622-50,705,799 , GRCh37.p13 chr17: 48,782,983-48,783,160 ANKRD40
    nsv6988772copy number variation1nstd229human GRCh38 chr17: 50,701,108-50,701,155 , GRCh37.p13 chr17: 48,778,469-48,778,516 ANKRD40
    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
    nsv6979859copy number variation1nstd229human GRCh38 chr17: 50,705,427-50,705,608 , GRCh37.p13 chr17: 48,782,788-48,782,969 ANKRD40
    nsv6581398inversion1nstd223human GRCh38 chr17: 50,706,344-50,706,900 , GRCh37.p13 chr17: 48,783,705-48,784,261 ANKRD40
    nsv6133067copy number variation1nstd213human GRCh37 chr17: 48,530,000-48,770,001 , GRCh38.p12 chr17: 50,452,639-50,692,640 CHAD, EPN3, 10 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5149016mobile element insertion1nstd203human GRCh38 chr17: 50,693,438-50,693,453 , GRCh37.p13 chr17: 48,770,799-48,770,814 ANKRD40
    nsv4418729copy number variation1nstd174human GRCh37 chr17: 48,777,951-48,778,735 , GRCh38.p12 chr17: 50,700,590-50,701,374 ANKRD40
    nsv4391813copy number variation1nstd171human GRCh37 chr17: 48,778,469-48,778,514 , GRCh38.p12 chr17: 50,701,108-50,701,153 ANKRD40
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4265532copy number variation1nstd166human GRCh37.p13 chr17: 48,775,000-48,783,000 , GRCh38.p12 chr17: 50,697,639-50,705,639 ANKRD40
    nsv4261703copy number variation1nstd166human GRCh37.p13 chr17: 48,782,788-48,782,969 , GRCh38.p12 chr17: 50,705,427-50,705,608 ANKRD40
    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
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