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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094978copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr17: 42,151,508-42,153,411 , GRCh38.p12 chr17: 44,074,140-44,076,043 HDAC5, G6PC3
    nsv6996771copy number variation1nstd229human GRCh38 chr17: 44,098,129-44,098,165 , GRCh37.p13 chr17: 42,175,497-42,175,533 HDAC5
    nsv6989022copy number variation1nstd229human GRCh38 chr17: 44,074,150-44,083,222 , GRCh37.p13 chr17: 42,151,518-42,160,590 HDAC5, G6PC3
    nsv6988569copy number variation1nstd229human GRCh38 chr17: 44,080,014-44,080,120 , GRCh37.p13 chr17: 42,157,382-42,157,488 HDAC5
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6507642copy number variation1nstd223human GRCh38 chr17: 44,112,910-44,113,334 , GRCh37.p13 chr17: 42,190,278-42,190,702 HDAC5
    nsv6507466copy number variation1nstd223human GRCh38 chr17: 44,074,150-44,083,219 , GRCh37.p13 chr17: 42,151,518-42,160,587 HDAC5, G6PC3
    nsv6502914copy number variation1nstd223human GRCh38 chr17: 44,102,121-44,106,473 , GRCh37.p13 chr17: 42,179,489-42,183,841 HDAC5
    nsv6291646copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,085,508-42,361,563 , GRCh38.p12 chr17: 44,008,140-44,284,195 LOC105371790, HDAC5, 16 more genes
    nsv6133311copy number variation3nstd213human GRCh37 chr17: 41,970,000-42,760,001 , GRCh38.p12 chr17: 43,892,632-44,682,633 FZD2, GRN, 43 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
    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
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