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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140034copy number variation1nstd232human GRCh37.p13 chr7: 56,126,212-56,126,309 , GRCh38.p12 chr7: 56,058,519-56,058,616 CCT6A, SNORA15
    nsv6836578copy number variation1nstd229human GRCh38 chr7: 56,052,371-56,136,871 , GRCh37.p13 chr7: 56,120,064-56,204,564 SNORA15, CCT6A, 6 more genes
    nsv6834298copy number variation1nstd229human GRCh38 chr7: 55,769,234-56,068,384 , GRCh37.p13 chr7: 55,836,927-56,136,077 ZNF713, LOC101409255, 12 more genes
    nsv6823794copy number variation1nstd229human GRCh38 chr7: 55,713,901-56,129,100 , GRCh37.p13 chr7: 55,781,594-56,196,793 SEPTIN14, LOC100419984, 23 more genes
    nsv6819940copy number variation1nstd229human GRCh38 chr7: 56,059,110-56,128,049 , GRCh37.p13 chr7: 56,126,803-56,195,742 NUPR2, SUMF2, 5 more genes
    nsv6636595copy number variation1nstd102humanUncertain significance GRCh37 chr7: 53,991,820-56,148,011 , GRCh38.p12 chr7: 53,924,127-56,080,318 PSPH, SNORA22B, 46 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632158copy number variation1nstd224human GRCh37 chr7: 56,106,397-56,146,310 , GRCh38.p12 chr7: 56,038,704-56,078,617 CCT6A, PHKG1, 4 more genes
    nsv6631902copy number variation1nstd224human GRCh37 chr7: 56,118,293-56,142,388 , GRCh38.p12 chr7: 56,050,600-56,074,695 CCT6A, SNORA22B, 3 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312780copy number variation2nstd102humanUncertain significance GRCh37 chr7: 56,079,455-56,174,106 , GRCh38.p12 chr7: 56,011,762-56,106,413 CCT6A, PSPH, 5 more genes
    nsv6291152copy number variation1nstd102humanLikely benign GRCh37 chr7: 55,757,106-56,489,653 , GRCh38.p12 chr7: 55,689,413-56,421,960 MRPS17, CCT6A, 43 more genes
    nsv6291142copy number variation1nstd102humanLikely benign GRCh37 chr7: 55,776,531-56,393,852 , GRCh38.p12 chr7: 55,708,838-56,326,159 SNORA15, CICP12, 29 more genes
    nsv6013062copy number variation1nstd212human GRCh38 chr7: 55,741,191-56,375,181 , GRCh37.p13 chr7: 55,808,884-56,442,874 , PSPH, 36 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5477528copy number variation1nstd206human GRCh38 chr7: 55,282,120-56,410,000 , GRCh37.p13 chr7: 55,349,813-56,477,693 , MRPS17, 52 more genes
    nsv5311687copy number variation1nstd204human GRCh37.p13 chr7: 56,127,698-56,127,834 , GRCh38.p13 chr7: 56,060,005-56,060,141 SNORA15, CCT6A
    nsv5237654copy number variation1nstd204human GRCh38.p13 chr7: 55,753,801-56,067,900 , GRCh37.p13 chr7: 55,821,494-56,135,593 ZNF713, SUMF2, 13 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964665copy number variation1nstd200human GRCh38 chr7: 56,052,371-56,136,871 , GRCh37.p13 chr7: 56,120,064-56,204,564 PHKG1, SUMF2, 6 more genes
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