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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5675968mobile element insertion2nstd211human GRCh38 chr7: 56,084,773-56,084,773 , GRCh37.p13 chr7: 56,152,466-56,152,466 PHKG1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5480275copy number variation1nstd206human GRCh38 chr7: 56,088,566-56,089,847 , GRCh37.p13 chr7: 56,156,259-56,157,540 PHKG1
    nsv5477528copy number variation1nstd206human GRCh38 chr7: 55,282,120-56,410,000 , GRCh37.p13 chr7: 55,349,813-56,477,693 , MRPS17, 52 more genes
    nsv5413871mobile element insertion1nstd206human GRCh38 chr7: 56,084,773-56,084,824 , GRCh37.p13 chr7: 56,152,466-56,152,517 PHKG1
    nsv5111995mobile element insertion1nstd203human GRCh38 chr7: 56,084,758-56,084,773 , GRCh37.p13 chr7: 56,152,451-56,152,466 PHKG1
    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
    nsv4956861copy number variation1nstd200human GRCh38 chr7: 56,082,606-56,084,226 , GRCh37.p13 chr7: 56,150,299-56,151,919 PHKG1
    nsv4819045copy number variation1nstd200human GRCh37 chr7: 56,150,299-56,151,919 , GRCh38.p12 chr7: 56,082,606-56,084,226 PHKG1
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4715977copy number variation1nstd195human GRCh37 chr7: 55,840,751-56,161,801 , GRCh38.p12 chr7: 55,773,058-56,094,108 SUMF2, CCT6A, 13 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
    nsv4490133mobile element insertion1nstd166human GRCh37.p13 chr7: 56,152,451-56,152,451 , GRCh38.p12 chr7: 56,084,758-56,084,758 PHKG1
    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
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