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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6832682copy number variation1nstd229human GRCh38 chr7: 43,517,622-43,536,989 , GRCh37.p13 chr7: 43,557,221-43,576,588 HECW1, LUARIS
    nsv6832549copy number variation1nstd229human GRCh38 chr7: 43,520,509-43,525,610 , GRCh37.p13 chr7: 43,560,108-43,565,209 HECW1, LUARIS
    nsv6829223copy number variation1nstd229human GRCh38 chr7: 43,507,778-43,507,967 , GRCh37.p13 chr7: 43,547,377-43,547,566 HECW1, LUARIS
    nsv6826787copy number variation1nstd229human GRCh38 chr7: 42,376,110-43,620,614 , GRCh37.p13 chr7: 42,415,709-43,660,213 LUARIS, PSMA2, 19 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
    nsv6136998copy number variation1nstd213human GRCh37 chr7: 43,200,000-43,920,001 , GRCh38.p12 chr7: 43,160,401-43,880,402 URGCP, HECW1-IT1, 12 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
    nsv5475762copy number variation1nstd206human GRCh38 chr7: 43,438,669-43,655,428 , GRCh37.p13 chr7: 43,478,268-43,695,027 LUARIS, HECW1, 2 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
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953626copy number variation1nstd200human GRCh38 chr7: 42,376,110-43,620,617 , GRCh37.p13 chr7: 42,415,709-43,660,216 TCP1P1, LOC105375250, 19 more genes
    nsv4676099copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,534,614-43,819,386 , GRCh38.p12 chr7: 43,495,015-43,779,787 LOC107986727, STK17A, 4 more genes
    nsv4456214copy number variation2nstd102humanUncertain significance GRCh37 chr7: 42,417,642-43,658,492 , GRCh38.p12 chr7: 42,378,043-43,618,893 RPL18AP10, LOC105375252, 19 more genes
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