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Items: 15

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    Number of Variants: 15

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3887144copy number variation1nstd102humanBenign GRCh37 chr6: 46,657,722-46,659,849 , GRCh38.p12 chr6: 46,689,985-46,692,112 TDRD6
    nsv3888600copy number variation1nstd102humanBenign GRCh37 chr6: 46,657,722-46,659,592 , GRCh38.p12 chr6: 46,689,985-46,691,855 TDRD6
    nsv3874249copy number variation1nstd102humanBenign GRCh37 chr6: 46,657,722-46,659,565 , GRCh38.p12 chr6: 46,689,985-46,691,828 TDRD6
    nsv3875786copy number variation1nstd102humanBenign GRCh37 chr6: 46,651,055-46,660,061 , GRCh38.p12 chr6: 46,683,318-46,692,324 TDRD6, TDRD6-AS1
    nsv3879963copy number variation1nstd102humanBenign GRCh37 chr6: 46,621,867-46,675,778 , GRCh38.p12 chr6: 46,654,130-46,708,041 TDRD6, TDRD6-AS1, 2 more genes
    nsv3923721copy number variation1nstd102humanPathogenic GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801 TDRD6, PAQR8, 131 more genes
    nsv3884243copy number variation1nstd102humanPathogenic GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607 TDRD6, GLYATL3, 105 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 TDRD6, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 TDRD6, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 TDRD6, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 TDRD6, ITPR3, 2905 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 TDRD6, HLA-DPB2, 1001 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TDRD6, TRR-ACG1-2, 1385 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 TDRD6, ACTG1P9, 245 more genes
    nsv3919465copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 45,061,475-48,062,533 , GRCh37 chr6: 44,953,497-47,954,574 , GRCh38 chr6: 44,985,760-47,986,838 TDRD6, ACTG1P9, 40 more genes
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