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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097765copy number variation1nstd102humanUncertain significance GRCh37 chr7: 96,318,236-97,493,828 , GRCh38.p12 chr7: 96,688,924-97,864,516 RN7SKP104, CZ1P-ASNS, 16 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv6636511copy number variation1nstd102humanPathogenic GRCh37 chr7: 96,264,152-96,860,892 , GRCh38.p12 chr7: 96,634,840-97,231,580 SDHAF3, DLX6, 9 more genes
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 more genes
    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
    nsv6312877copy number variation1nstd102humanPathogenic GRCh37 chr7: 95,434,042-96,747,209 , GRCh38.p12 chr7: 95,804,730-97,117,897 DYNC1I1, DLX6-AS1, 18 more genes
    nsv6137024copy number variation1nstd213human GRCh37 chr7: 93,400,000-97,690,001 , GRCh38.p12 chr7: 93,770,688-98,060,689 , SEM1, 77 more genes
    nsv6136282copy number variation1nstd213human GRCh37 chr7: 96,390,000-97,020,001 , GRCh38.p12 chr7: 96,760,688-97,390,689 DLX5, MARK2P10, 10 more genes
    nsv6135798copy number variation1nstd213human GRCh37 chr7: 96,600,000-97,000,001 , GRCh38.p12 chr7: 96,970,688-97,370,689 DLX5, DLX6, 7 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
    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
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 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
    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
    nsv4685991copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 95,911,538-97,301,820 , GRCh38.p12 chr7: 96,282,226-97,672,508 DLX5, DLX6, 22 more genes
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