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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976519inversion1nstd209human GRCh38 chr7: 63,374,409-63,521,610 , GRCh37.p13 chr7: 62,834,787-62,981,988 , ARAFP2, 9 more genes
    nsv5973368inversion1nstd209human GRCh38 chr7: 63,246,026-63,525,509 , GRCh37.p13 chr7: 62,706,404-62,985,887 , ARAFP3, 17 more genes
    nsv5669339inversion1nstd207human GRCh37.p13 chr7: 62,752,532-63,107,579 , GRCh38 chr7: 63,292,154-63,647,201 , TNRC18P2, 19 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5485319copy number variation1nstd206human GRCh38 chr7: 63,390,779-63,402,779 , GRCh37.p13 chr7: 62,851,157-62,863,157 , ARAFP2, 4 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4957415copy number variation1nstd200human GRCh38 chr7: 63,162,835-63,881,030 , GRCh37.p13 chr7: 62,623,213-63,341,408 , VN1R32P, 31 more genes
    nsv4765725inversion1nstd199human GRCh37 chr7: 57,119,077-62,979,736 , GRCh38.p12 chr7: 57,051,370-63,519,358 , ZNF479, 70 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4753662inversion1nstd199human GRCh37 chr7: 62,748,716-62,918,281 , GRCh38.p12 chr7: 63,288,338-63,457,903 , ARAFP3, 14 more genes
    nsv4730143inversion19nstd198human GRCh37.p13 chr7: 62,779,707-62,885,103 , GRCh38 chr7: 63,319,329-63,424,725 , ARAFP3, 12 more genes
    nsv4729639copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,508,852-64,940,346 , GRCh38.p12 chr7: 63,048,474-65,475,433 VN1R39P, LOC105375324, 113 more genes
    nsv4728981copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,495,083-64,927,758 , GRCh38.p12 chr7: 63,034,705-65,462,845 LOC105375321, GUSBP6, 113 more genes
    nsv4607832copy number variation1nstd183human GRCh37 chr7: 62,026,983-62,925,064 , GRCh38.p12 chr7: 62,566,605-63,464,686 , RNU6-417P, 22 more genes
    nsv4606786copy number variation1nstd183human GRCh37 chr7: 62,520,372-64,227,496 , GRCh38.p12 chr7: 63,059,994-64,767,118 , LOC105375326, 89 more genes
    nsv4524480copy number variation1nstd166human GRCh37.p13 chr7: 62,803,999-62,868,000 , GRCh38.p12 chr7: 63,343,621-63,407,622 , LOC102724738, 12 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4410047copy number variation1nstd174human GRCh37 chr7: 61,728,395-62,984,310 , GRCh38.p12 chr7: 58,068,645-62,294,432 , GRCh38.p12 chr7: 58,088,705-62,376,074 , GRCh38.p12 chr7: 62,294,433-63,523,932 , PHKG1P1, 25 more genes
    nsv4409176copy number variation1nstd174human GRCh37 chr7: 62,589,161-63,109,895 , GRCh38.p12 chr7: 63,128,783-63,649,517 , ARAFP3, 23 more genes
    nsv4408245copy number variation1nstd174human GRCh37 chr7: 62,181,098-62,879,551 , GRCh38.p12 chr7: 62,720,720-63,419,173 , SAPCD2P4, 21 more genes
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