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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047217inversion1nstd229human GRCh38 chr6: 26,281,994-26,284,094 , GRCh37.p13 chr6: 26,282,222-26,284,322 H4C8
    nsv6797790copy number variation1nstd229human GRCh38 chr6: 26,236,594-26,309,109 , GRCh37.p13 chr6: 26,236,822-26,309,337 H2BC9, H2AC10P, 10 more genes
    nsv6792601copy number variation1nstd229human GRCh38 chr6: 26,035,437-26,331,519 , GRCh37.p13 chr6: 26,035,665-26,331,747 TRS-AGA2-1, H2AC8, 49 more genes
    nsv6789683copy number variation1nstd229human GRCh38 chr6: 26,281,973-26,298,106 , GRCh37.p13 chr6: 26,282,201-26,298,334 H4C8, TRX-CAT1-2, 1 more genes
    nsv6789669copy number variation1nstd229human GRCh38 chr6: 25,978,117-26,742,203 , GRCh37.p13 chr6: 25,978,345-26,585,842 H2AC8, BTN1A1P1, 93 more genes
    nsv6787290copy number variation1nstd229human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 CARMIL1, H2AC8, 74 more genes
    nsv6779975copy number variation1nstd229human GRCh38 chr6: 26,174,832-26,350,330 , GRCh37.p13 chr6: 26,175,060-26,350,558 TRQ-TTG3-2, LOC101928743, 36 more genes
    nsv6563406inversion1nstd223human GRCh38 chr6: 25,888,425-29,704,317 , GRCh37.p13 chr6: 25,888,653-29,672,094 OR1F12P, H4C2, 362 more genes
    nsv6402318copy number variation1nstd223human GRCh38 chr6: 25,240,953-26,330,257 , GRCh37.p13 chr6: 25,241,181-26,330,485 H2BC7, H2AC7, 74 more genes
    nsv6396289copy number variation1nstd223human GRCh38 chr6: 26,236,593-26,320,113 , GRCh37.p13 chr6: 26,236,821-26,320,341 H4C8, H2BC10, 16 more genes
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4940474copy number variation1nstd200human GRCh38 chr6: 26,236,593-26,320,115 , GRCh37.p13 chr6: 26,236,821-26,320,343 , H2BC10, 17 more genes
    nsv4940473copy number variation1nstd200human GRCh38 chr6: 26,236,594-26,309,109 , GRCh37.p13 chr6: 26,236,822-26,309,337 , TRR-TCG4-1, 11 more genes
    nsv4934536copy number variation1nstd200human GRCh38 chr6: 26,150,781-26,331,570 , GRCh37.p13 chr6: 26,151,009-26,331,798 , LARP1P1, 41 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4729341copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965 H1-4, TRV-CAC1-6, 78 more genes
    nsv4675352copy number variation1nstd102humanLikely benign GRCh37 chr6: 26,238,509-26,329,714 , GRCh38.p12 chr6: 26,238,281-26,329,486 H3C9P, TRQ-TTG3-2, 22 more genes
    nsv4675256copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,256,525-26,536,884 , GRCh38.p12 chr6: 26,256,297-26,536,656 LOC101928743, TRQ-TTG3-2, 35 more genes
    nsv4598438copy number variation1nstd183human GRCh37 chr6: 26,103,998-26,365,563 , GRCh38.p12 chr6: 26,103,770-26,365,335 , H2AC10P, 46 more genes
    nsv4593441copy number variation1nstd183human GRCh37 chr6: 26,153,284-26,321,490 , GRCh38.p12 chr6: 26,153,056-26,321,262 , H2BC9, 35 more genes
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