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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482838copy number variation1nstd206human GRCh38 chr7: 56,103,219-56,103,287 , GRCh37.p13 chr7: 56,170,912-56,170,980 CHCHD2
    nsv5481996copy number variation1nstd206human GRCh38 chr7: 56,106,327-56,106,436 , GRCh37.p13 chr7: 56,174,020-56,174,129 CHCHD2
    nsv5477528copy number variation1nstd206human GRCh38 chr7: 55,282,120-56,410,000 , GRCh37.p13 chr7: 55,349,813-56,477,693 , MRPS17, 52 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964665copy number variation1nstd200human GRCh38 chr7: 56,052,371-56,136,871 , GRCh37.p13 chr7: 56,120,064-56,204,564 PHKG1, SUMF2, 6 more genes
    nsv4956864copy number variation1nstd200human GRCh38 chr7: 56,104,002-56,106,736 , GRCh37.p13 chr7: 56,171,695-56,174,429 CHCHD2
    nsv4956863copy number variation1nstd200human GRCh38 chr7: 56,098,920-56,102,576 , GRCh37.p13 chr7: 56,166,613-56,170,269 CHCHD2
    nsv4819048copy number variation1nstd200human GRCh37 chr7: 56,166,613-56,170,269 , GRCh38.p12 chr7: 56,098,920-56,102,576 CHCHD2
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4709456copy number variation1nstd195human GRCh37 chr7: 56,165,301-56,217,701 , GRCh38.p12 chr7: 56,097,608-56,150,008 CHCHD2, NUPR2, 1 more genes
    nsv4616998copy number variation1nstd183human GRCh37 chr7: 56,155,561-56,330,552 , GRCh38.p12 chr7: 56,087,868-56,262,859 PHKG1, CHCHD2, 5 more genes
    nsv4612052copy number variation1nstd183human GRCh37 chr7: 56,155,087-56,326,872 , GRCh38.p12 chr7: 56,087,394-56,259,179 PHKG1, CHCHD2, 5 more genes
    nsv4611432copy number variation2nstd183human GRCh37 chr7: 55,619,800-56,385,412 , GRCh38.p12 chr7: 55,552,107-56,317,719 , LOC101928755, 37 more genes
    nsv4578666copy number variation1nstd102humanUncertain significance GRCh37 chr7: 56,169,544-56,174,106 , GRCh38.p12 chr7: 56,101,851-56,106,413 CHCHD2
    nsv4455806copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,809,787-58,025,873 , GRCh38.p12 chr7: 52,742,093-57,966,167 RPL31P35, SEC61G, 161 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
    nsv4411705copy number variation1nstd174human GRCh37 chr7: 56,031,072-56,186,821 , GRCh38.p12 chr7: 55,963,379-56,119,128 CCT6A, NIPSNAP2, 8 more genes
    nsv4400210copy number variation1nstd174human GRCh37 chr7: 55,619,800-56,483,244 , GRCh38.p12 chr7: 55,552,107-56,415,551 , PHKG1, 49 more genes
    nsv4394401copy number variation1nstd174human GRCh37 chr7: 56,117,100-56,632,479 , GRCh38.p12 chr7: 56,049,407-56,564,786 IFITM3P4, VN1R25P, 34 more genes
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