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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097375copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,810,758-44,747,598 , GRCh38.p12 chr7: 43,771,159-44,707,999 RASA4CP, OGDH, 31 more genes
    nsv6836124copy number variation1nstd229human GRCh38 chr7: 44,073,396-44,080,253 , GRCh37.p13 chr7: 44,112,995-44,119,852 MIR6838, POLM
    nsv6829096copy number variation1nstd229human GRCh38 chr7: 44,065,842-44,074,676 , GRCh37.p13 chr7: 44,105,441-44,114,275 PGAM2, DBNL, 2 more genes
    nsv6825178copy number variation1nstd229human GRCh38 chr7: 44,006,401-44,163,300 , GRCh37.p13 chr7: 44,046,000-44,202,899 PGAM2, POLR2J4, 14 more genes
    nsv6824378copy number variation1nstd229human GRCh38 chr7: 43,852,301-44,460,500 , GRCh37.p13 chr7: 43,891,900-44,500,099 DBNL, GCK, 23 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
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6136183copy number variation1nstd213human GRCh37 chr7: 43,240,000-44,280,001 , GRCh38.p12 chr7: 43,200,401-44,240,402 GCK, YKT6, 31 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 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
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5109866mobile element insertion1nstd203human GRCh38 chr7: 44,081,467-44,081,476 , GRCh37.p13 chr7: 44,121,066-44,121,075 POLM
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956419copy number variation1nstd200human GRCh38 chr7: 44,082,658-44,083,708 , GRCh37.p13 chr7: 44,122,257-44,123,307 POLM
    nsv4953631copy number variation1nstd200human GRCh38 chr7: 44,065,842-44,074,681 , GRCh37.p13 chr7: 44,105,441-44,114,280 PGAM2, DBNL, 2 more genes
    nsv4828891copy number variation1nstd200human GRCh37 chr7: 44,105,441-44,114,280 , GRCh38.p12 chr7: 44,065,842-44,074,681 POLM, DBNL, 2 more genes
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