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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7038651inversion1nstd229human GRCh38 chr7: 56,300,383-56,471,357 , GRCh37.p13 chr7: 56,368,076-56,539,050 LOC105375292, LOC728376, 13 more genes
    nsv6834252copy number variation1nstd229human GRCh38 chr7: 56,283,001-56,365,200 , GRCh37.p13 chr7: 56,350,694-56,432,893 CICP8, LOC154937, 4 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
    nsv6833136copy number variation1nstd229human GRCh38 chr7: 56,117,468-56,307,848 , GRCh37.p13 chr7: 56,185,161-56,375,541 LOC154937, LOC105375288, 4 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
    nsv6616301copy number variation1nstd223human GRCh38 chr7: 56,152,555-56,321,885 , GRCh37.p13 chr7: 56,220,248-56,389,578 CCNJP1, IFITM3P4, 3 more genes
    nsv6603556copy number variation1nstd223human GRCh38 chr7: 56,283,073-56,338,016 , GRCh37.p13 chr7: 56,350,766-56,405,709 LOC154937, LOC441228
    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
    nsv6013062copy number variation1nstd212human GRCh38 chr7: 55,741,191-56,375,181 , GRCh37.p13 chr7: 55,808,884-56,442,874 , PSPH, 36 more genes
    nsv6006610copy number variation1nstd212human GRCh37.p13 chr7: 56,185,161-56,375,542 , GRCh38 chr7: 56,117,468-56,307,849 LOC154937, LOC441228, 4 more genes
    nsv5729685mobile element insertion2nstd211human GRCh38 chr7: 56,305,289-56,305,289 , GRCh37.p13 chr7: 56,372,982-56,372,982 LOC154937
    nsv5557178mobile element insertion1nstd206human GRCh38 chr7: 56,305,305-56,305,340 , GRCh37.p13 chr7: 56,372,998-56,373,033 LOC154937
    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
    nsv5197165mobile element insertion1nstd203human GRCh38 chr7: 56,301,946-56,301,963 , GRCh37.p13 chr7: 56,369,639-56,369,656 LOC154937
    nsv5192317mobile element insertion1nstd203human GRCh38 chr7: 56,301,951-56,301,963 , GRCh37.p13 chr7: 56,369,644-56,369,656 LOC154937
    nsv5190030mobile element insertion1nstd203human GRCh38 chr7: 56,301,952-56,301,963 , GRCh37.p13 chr7: 56,369,645-56,369,656 LOC154937
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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