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Items: 1 to 20 of 772

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6635532copy number variation1nstd227human GRCh38.p12 chr16: 35,069,552-35,532,147 , GRCh37 chr16: 34,303,923-34,766,518 FRG2DP, LINC01566, 37 more genes
    nsv6635401copy number variation3nstd227human GRCh38.p12 chr16: 35,281,704-35,512,674 , GRCh37 chr16: 34,516,075-34,747,045 FRG2DP, LINC01566, 20 more genes
    nsv6635257copy number variation1nstd227human GRCh38.p12 chr16: 35,182,462-35,582,805 , GRCh37 chr16: 34,416,833-34,817,176 FRG2DP, LINC01566, 33 more genes
    nsv6623666copy number variation2nstd224human GRCh37 chr16: 34,516,075-34,779,801 , GRCh38.p12 chr16: 35,281,704-35,545,430 ZNF971P, C2orf69P4, 21 more genes
    nsv6623665copy number variation1nstd224human GRCh37 chr16: 34,489,371-34,814,298 , GRCh38.p12 chr16: 35,255,000-35,579,927 FRG2DP, C2orf69P2, 27 more genes
    nsv6623618copy number variation1nstd224human GRCh37 chr16: 34,516,075-35,111,521 , GRCh38.p12 chr16: 35,281,704-35,877,150 KIF18BP1, RNA5SP407, 46 more genes
    nsv6623617copy number variation1nstd224human GRCh37 chr16: 34,516,075-34,781,023 , GRCh38.p12 chr16: 35,281,704-35,546,652 FRG2DP, C2orf69P2, 22 more genes
    nsv6623616copy number variation3nstd224human GRCh37 chr16: 34,516,075-34,766,518 , GRCh38.p12 chr16: 35,281,704-35,532,147 ZNF971P, C2orf69P4, 20 more genes
    nsv6623614copy number variation36nstd224human GRCh37 chr16: 34,489,371-34,740,580 , GRCh38.p12 chr16: 35,255,000-35,506,209 LINC01566, AGGF1P9, 23 more genes
    nsv6623468copy number variation1nstd224human GRCh37 chr16: 34,599,473-35,257,261 , GRCh38.p12 chr16: 35,365,102-36,022,890 RNA5SP407, RNA5SP410, 41 more genes
    nsv6623467copy number variation1nstd224human GRCh37 chr16: 34,533,419-34,740,580 , GRCh38.p12 chr16: 35,299,048-35,506,209 FRG2DP, C2orf69P2, 20 more genes
    nsv6623464copy number variation2nstd224human GRCh37 chr16: 34,179,316-35,257,261 , GRCh38.p12 chr16: 34,944,945-36,022,890 LOC162137, LINC01566, 68 more genes
    nsv6623449copy number variation1nstd224human GRCh37 chr16: 32,221,291-34,740,580 , GRCh38.p12 chr16: 32,209,970-35,506,209 IGHV3OR16-12, FRG2DP, 111 more genes
    nsv6623221copy number variation1nstd224human GRCh37 chr16: 34,686,820-35,111,521 , GRCh38.p12 chr16: 35,452,449-35,877,150 LINC02167, HMGN2P41, 31 more genes
    nsv6290072copy number variation1nstd218human GRCh38.p12 chr16: 34,632,766-36,225,009 , GRCh38.p12 chr7: 61,006,478-62,429,617 , GRCh38.p12 chr1: 146,347,888-148,514,931 , GRCh37 chr1: 147,806,599-149,821,717 , BCL9, 149 more genes
    nsv6133197copy number variation1nstd213human GRCh37 chr16: 34,180,000-35,280,001 , GRCh38.p12 chr16: 34,945,629-36,045,630 FRG2DP, LOC162137, 68 more genes
    nsv6133024copy number variation1nstd213human GRCh37 chr16: 34,440,000-34,750,001 , GRCh38.p12 chr16: 35,205,629-35,515,630 LINC01566, C2orf69P2, 28 more genes
    nsv6132988copy number variation1nstd213human GRCh37 chr16: 34,480,000-34,760,001 , GRCh38.p12 chr16: 35,245,629-35,525,630 LINC01566, AGGF1P9, 24 more genes
    nsv6132987copy number variation1nstd213human GRCh37 chr16: 34,420,000-34,820,001 , GRCh38.p12 chr16: 35,185,629-35,585,630 C2orf69P1, AGGF1P5, 33 more genes
    nsv6132986copy number variation1nstd213human GRCh37 chr16: 34,180,000-35,250,001 , GRCh38.p12 chr16: 34,945,629-36,015,630 FRG2DP, LOC162137, 68 more genes
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