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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098141copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,830,050-91,867,093 , GRCh38.p12 chr7: 92,200,736-92,237,779 KRIT1, MIR1285-1
    nsv7097391copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,830,050-91,844,111 , GRCh38.p12 chr7: 92,200,736-92,214,797 KRIT1, MIR1285-1
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv6831735copy number variation1nstd229human GRCh38 chr7: 92,060,601-92,295,600 , GRCh37.p13 chr7: 91,689,915-91,924,914 CYP51A1, ANKIB1, 5 more genes
    nsv6823692copy number variation1nstd229human GRCh38 chr7: 92,202,670-92,203,022 , GRCh37.p13 chr7: 91,831,984-91,832,336 KRIT1, MIR1285-1
    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
    nsv6312462copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,830,690-91,832,501 , GRCh38.p12 chr7: 92,201,376-92,203,187 MIR1285-1, KRIT1
    nsv6137820copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,715,729-91,972,337 , GRCh38.p12 chr7: 92,086,415-92,343,023 KRIT1, CYP51A1, 5 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
    nsv5673851copy number variation1nstd102humanPathogenic GRCh37 chr7: 91,829,918-91,851,387 , GRCh38.p12 chr7: 92,200,604-92,222,073 MIR1285-1, KRIT1
    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
    nsv4964960copy number variation1nstd200human GRCh38 chr7: 92,148,896-92,215,642 , GRCh37.p13 chr7: 91,778,210-91,844,956 KRIT1, LRRD1, 2 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825162copy number variation1nstd200human GRCh37 chr7: 91,778,210-91,844,956 , GRCh38.p12 chr7: 92,148,896-92,215,642 CYP51A1-AS1, MIR1285-1, 2 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
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