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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6833549copy number variation1nstd229human GRCh38 chr7: 56,076,822-56,576,436 , GRCh37.p13 chr7: 56,144,515-56,644,129 NMD3P2, RNU6-1052P, 31 more genes
    nsv6829251copy number variation1nstd229human GRCh38 chr7: 56,116,727-56,264,851 , GRCh37.p13 chr7: 56,184,420-56,332,544 IFITM3P4, LOC100130909, 3 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
    nsv6822281copy number variation1nstd229human GRCh38 chr7: 56,071,901-56,125,400 , GRCh37.p13 chr7: 56,139,594-56,193,093 SUMF2, CHCHD2, 3 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
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6610409copy number variation1nstd223human GRCh38 chr7: 56,116,727-56,264,851 , GRCh37.p13 chr7: 56,184,420-56,332,544 IFITM3P4, LOC100130909, 3 more genes
    nsv6601066copy number variation1nstd223human GRCh38 chr7: 56,115,694-56,121,513 , GRCh37.p13 chr7: 56,183,387-56,189,206 NUPR2, LOC105375288
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6070188insertion1nstd212human GRCh38 chr7: 56,115,413-56,115,413 , GRCh37.p13 chr7: 56,183,106-56,183,106 NUPR2
    nsv6064571insertion1nstd212human GRCh38 chr7: 56,115,625-56,115,625 , GRCh37.p13 chr7: 56,183,318-56,183,318 NUPR2
    nsv6013062copy number variation1nstd212human GRCh38 chr7: 55,741,191-56,375,181 , GRCh37.p13 chr7: 55,808,884-56,442,874 , PSPH, 36 more genes
    nsv5952738insertion1nstd209human GRCh38 chr7: 56,115,429-56,115,429 , GRCh37.p13 chr7: 56,183,122-56,183,122 NUPR2
    nsv5920616copy number variation1nstd209human GRCh38 chr7: 56,116,275-56,116,330 , GRCh37.p13 chr7: 56,183,968-56,184,023 NUPR2
    nsv5634616insertion1nstd207human GRCh38 chr7: 56,115,413-56,115,413 , GRCh37.p13 chr7: 56,183,106-56,183,106 NUPR2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5540764insertion1nstd206human GRCh38 chr7: 56,115,428-56,115,455 , GRCh37.p13 chr7: 56,183,121-56,183,148 NUPR2
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