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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049777inversion1nstd229human GRCh38 chr7: 91,857,662-91,893,542 , GRCh37.p13 chr7: 91,486,976-91,522,856 MTERF1, LOC112267986
    nsv7045086inversion1nstd229human GRCh38 chr7: 91,878,401-91,880,285 , GRCh37.p13 chr7: 91,507,715-91,509,599 LOC112267986, MTERF1
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv7042235inversion1nstd229human GRCh38 chr7: 91,883,552-91,893,871 , GRCh37.p13 chr7: 91,512,866-91,523,185 LOC112267986
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6136278copy number variation1nstd213human GRCh37 chr7: 91,430,000-91,610,001 , GRCh38.p12 chr7: 91,800,686-91,980,687 MTERF1, AKAP9, 1 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv5563019sequence alteration1nstd206human GRCh38 chr7: 91,857,662-91,893,869 , GRCh37.p13 chr7: 91,486,976-91,523,183 MTERF1, LOC112267986
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4957643copy number variation1nstd200human GRCh38 chr7: 91,882,311-91,911,701 , GRCh37.p13 chr7: 91,511,625-91,541,015 LOC112267986
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4616941copy number variation1nstd183human GRCh37 chr7: 91,170,449-91,743,150 , GRCh38.p12 chr7: 91,541,134-92,113,836 MTERF1, CYP51A1, 2 more genes
    nsv4523924copy number variation1nstd166human GRCh37.p13 chr7: 90,941,478-91,732,937 , GRCh38.p12 chr7: 91,312,163-92,103,623 MTERF1, AKAP9, 5 more genes
    nsv4485355mobile element insertion1nstd166human GRCh37.p13 chr7: 91,509,256-91,509,256 , GRCh38.p12 chr7: 91,879,942-91,879,942 LOC112267986, MTERF1
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