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Items: 1 to 20 of 77

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5725198mobile element insertion1nstd211human GRCh38 chr6: 47,823,279-47,823,279 , GRCh37.p13 chr6: 47,791,015-47,791,015 RNU1-105P, OPN5
    nsv5561064mobile element insertion1nstd206human GRCh38 chr6: 47,823,279-47,823,330 , GRCh37.p13 chr6: 47,791,015-47,791,066 OPN5, RNU1-105P
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5162264mobile element insertion1nstd203human GRCh38 chr6: 47,823,263-47,823,279 , GRCh37.p13 chr6: 47,790,999-47,791,015 RNU1-105P, OPN5
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4558908mobile element insertion1nstd166human GRCh37.p13 chr6: 47,790,999-47,790,999 , GRCh38.p12 chr6: 47,823,263-47,823,263 OPN5, RNU1-105P
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 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 PAQR8, GSTA6P, 131 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 ACTG1P9, RUNX2, 40 more genes
    nsv3913758copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 47,267,474-51,400,063 , GRCh37 chr6: 47,159,515-51,292,104 , GRCh38 chr6: 47,191,779-51,427,306 CRISP1, FTH1P5, 46 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3884243copy number variation1nstd102humanPathogenic GRCh37 chr6: 43,636,308-50,947,320 , GRCh38.p12 chr6: 43,668,571-50,979,607 GLYATL3, RNU6-754P, 105 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
    nsv3168805inversion1nstd158human GRCh37 chr6: 12,296,990-80,059,394 , GRCh38.p12 chr6: 12,296,757-79,349,677 , ABCF1, 1548 more genes
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