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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5374933translocation1nstd200human GRCh38 chr18: 35,498,379-35,498,379 , GRCh38 chr17: 44,078,294-44,078,294 , GRCh37.p13 chr17: 42,155,662-42,155,662 , GRCh37.p13 chr18: 33,078,343-33,078,343 HDAC5, INO80C
    nsv5358883translocation1nstd200human GRCh38 chr17: 44,102,512-44,102,512 , GRCh38 chr17: 44,108,080-44,108,080 , GRCh37.p13 chr17: 42,185,448-42,185,448 , GRCh37.p13 chr17: 42,179,880-42,179,880 HDAC5
    nsv5327785copy number variation1nstd204human GRCh38.p13 chr17: 44,103,845-44,106,683 , GRCh37.p13 chr17: 42,181,213-42,184,051 HDAC5
    nsv5215057mobile element deletion1nstd204human GRCh38.p13 chr17: 44,101,116-44,101,434 , GRCh37.p13 chr17: 42,178,484-42,178,802 HDAC5
    nsv5016505copy number variation1nstd200human GRCh38 chr17: 44,102,575-44,103,877 , GRCh37.p13 chr17: 42,179,943-42,181,245 HDAC5
    nsv5016504copy number variation1nstd200human GRCh38 chr17: 44,100,332-44,100,397 , GRCh37.p13 chr17: 42,177,700-42,177,765 HDAC5
    nsv5016503copy number variation1nstd200human GRCh38 chr17: 44,099,598-44,100,814 , GRCh37.p13 chr17: 42,176,966-42,178,182 HDAC5
    nsv5013734copy number variation1nstd200human GRCh38 chr17: 44,074,150-44,083,222 , GRCh37.p13 chr17: 42,151,518-42,160,590 G6PC3, HDAC5
    nsv4907346mobile element deletion1nstd200human GRCh38 chr17: 44,101,125-44,101,426 , GRCh37.p13 chr17: 42,178,493-42,178,794 HDAC5
    nsv4867080copy number variation1nstd200human GRCh37 chr17: 42,179,943-42,181,245 , GRCh38.p12 chr17: 44,102,575-44,103,877 HDAC5
    nsv4864669copy number variation1nstd200human GRCh37 chr17: 42,151,518-42,160,590 , GRCh38.p12 chr17: 44,074,150-44,083,222 HDAC5, G6PC3
    nsv4769504mobile element deletion1nstd200human GRCh37 chr17: 42,178,493-42,178,794 , GRCh38.p12 chr17: 44,101,125-44,101,426 HDAC5
    nsv4681862copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,105,175-42,430,244 , GRCh38.p12 chr17: 44,027,807-44,352,876 G6PC3, ATXN7L3, 21 more genes
    nsv4680708copy number variation1nstd189human GRCh37.p13 chr17: 41,357,686-42,167,307 , GRCh38.p12 chr17: 43,205,667-44,089,939 , ARL4D, 41 more genes
    nsv4673782copy number variation2nstd186human GRCh37 chr17: 42,200,991-42,201,037 , GRCh38.p12 chr17: 44,123,623-44,123,669 HDAC5
    nsv4634357copy number variation2nstd183human GRCh37 chr17: 42,200,991-42,201,037 , GRCh38.p12 chr17: 44,123,623-44,123,669 HDAC5
    nsv4368311copy number variation1nstd173human GRCh37 chr17: 41,384,516-42,395,351 , GRCh38.p12 chr17: 43,307,154-44,317,983 , LOC105371789, 55 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4270167copy number variation1nstd166human GRCh37.p13 chr17: 42,171,828-42,178,502 , GRCh38.p12 chr17: 44,094,460-44,101,134 HDAC5
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