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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148127copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,973,263-14,669,896 , GRCh38.p12 chr7: 10,933,636-14,630,271 LOC105375162, LOC105375156, 33 more genes
    nsv7056755inversion1nstd229human GRCh38 chr7: 12,676,462-12,938,634 , GRCh37.p13 chr7: 12,716,087-12,978,259 RBMX2P4, LOC100505995, 3 more genes
    nsv7054063inversion1nstd229human GRCh38 chr7: 7,723,636-12,911,662 , GRCh37.p13 chr7: 7,763,267-12,951,287 NXPH1, CCNB2P1, 50 more genes
    nsv7053494inversion1nstd229human GRCh38 chr7: 12,155,513-12,915,637 , GRCh37.p13 chr7: 12,195,139-12,955,262 SCIN, RN7SKP228, 13 more genes
    nsv7049984inversion1nstd229human GRCh38 chr7: 11,159,456-12,799,960 , GRCh37.p13 chr7: 11,199,083-12,839,585 THSD7A, LOC105375156, 17 more genes
    nsv6816537copy number variation1nstd229human GRCh38 chr7: 12,612,636-13,225,383 , GRCh37.p13 chr7: 12,652,261-13,265,008 ARL4A, LOC105375157, 5 more genes
    nsv6809848copy number variation1nstd229human GRCh38 chr7: 12,672,201-12,700,000 , GRCh37.p13 chr7: 12,711,826-12,739,625 LOC100505995, ARL4A, 1 more genes
    nsv6806146copy number variation1nstd229human GRCh38 chr7: 12,676,454-12,920,642 , GRCh37.p13 chr7: 12,716,079-12,960,267 LOC100505995, ARL4A, 2 more genes
    nsv6805090copy number variation1nstd229human GRCh38 chr7: 11,673,765-12,709,856 , GRCh37.p13 chr7: 11,713,392-12,749,481 TAS2R2P, LOC105375155, 14 more genes
    nsv6637142copy number variation1nstd102humanUncertain significance GRCh37 chr7: 12,479,868-13,696,843 , GRCh38.p12 chr7: 12,440,242-13,657,218 LOC107986770, ARL4A, 13 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 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
    nsv6615376copy number variation1nstd223human GRCh38 chr7: 12,686,501-12,687,900 , GRCh37.p13 chr7: 12,726,126-12,727,525 LOC100505995, ARL4A
    nsv6604753copy number variation1nstd223human GRCh38 chr7: 12,686,601-12,687,200 , GRCh37.p13 chr7: 12,726,226-12,726,825 ARL4A, LOC100505995
    nsv6603296copy number variation1nstd223human GRCh38 chr7: 12,042,870-12,685,584 , GRCh37.p13 chr7: 12,082,496-12,725,209 LOC105375155, SSBL5P, 12 more genes
    nsv6571367inversion1nstd223human GRCh38 chr7: 12,550,789-13,575,895 , GRCh37.p13 chr7: 12,590,415-13,615,520 ARL4A, SCIN, 7 more genes
    nsv6566816inversion1nstd223human GRCh38 chr7: 12,550,873-13,575,818 , GRCh37.p13 chr7: 12,590,499-13,615,443 ARL4A, SCIN, 7 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313854copy number variation1nstd102humanPathogenic GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463 LOC107986766, RPL36AP26, 115 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
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