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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048488inversion1nstd229human GRCh38 chr7: 92,114,194-92,116,239 , GRCh37.p13 chr7: 91,743,508-91,745,553 CYP51A1
    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
    nsv6830284copy number variation1nstd229human GRCh38 chr7: 92,113,245-92,114,411 , GRCh37.p13 chr7: 91,742,559-91,743,725 AKAP9, CYP51A1
    nsv6821440copy number variation1nstd229human GRCh38 chr7: 92,114,814-92,114,914 , GRCh37.p13 chr7: 91,744,128-91,744,228 CYP51A1
    nsv6820894copy number variation1nstd229human GRCh38 chr7: 92,115,701-92,122,000 , GRCh37.p13 chr7: 91,745,015-91,751,314 CYP51A1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632475copy number variation1nstd224human GRCh37 chr7: 91,764,054-91,780,003 , GRCh38.p12 chr7: 92,134,740-92,150,689 CYP51A1, LRRD1, 1 more genes
    nsv6615409copy number variation1nstd223human GRCh38 chr7: 92,129,101-92,133,100 , GRCh37.p13 chr7: 91,758,415-91,762,414 CYP51A1-AS1, CYP51A1
    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
    nsv6257482mobile element insertion1nstd215human GRCh38 chr7: 92,122,238-92,122,238 , GRCh37.p13 chr7: 91,751,552-91,751,552 CYP51A1
    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
    nsv6063919insertion1nstd212human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
    nsv5950465insertion1nstd209human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
    nsv5675872mobile element insertion2nstd211human GRCh38 chr7: 92,122,238-92,122,238 , GRCh37.p13 chr7: 91,751,552-91,751,552 CYP51A1
    nsv5627189insertion1nstd207human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5403465mobile element insertion1nstd206human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
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