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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7051552inversion1nstd229human GRCh38 chr6: 11,086,774-14,472,374 , GRCh37.p13 chr6: 11,087,007-14,472,605 LOC105374933, ADTRP, 53 more genes
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6792537copy number variation1nstd229human GRCh38 chr6: 11,683,657-11,688,406 , GRCh37.p13 chr6: 11,683,890-11,688,639 LOC340184
    nsv6788951copy number variation1nstd229human GRCh38 chr6: 11,708,680-11,709,104 , GRCh37.p13 chr6: 11,708,913-11,709,337 LOC340184
    nsv6787714copy number variation1nstd229human GRCh38 chr6: 11,675,101-11,729,500 , GRCh37.p13 chr6: 11,675,334-11,729,733 ADTRP, LOC340184
    nsv6786746copy number variation1nstd229human GRCh38 chr6: 11,705,014-11,705,381 , GRCh37.p13 chr6: 11,705,247-11,705,614 LOC340184
    nsv6783089copy number variation1nstd229human GRCh38 chr6: 11,675,030-11,729,571 , GRCh37.p13 chr6: 11,675,263-11,729,804 LOC340184, ADTRP
    nsv6782024copy number variation1nstd229human GRCh38 chr6: 11,691,244-11,700,692 , GRCh37.p13 chr6: 11,691,477-11,700,925 LOC340184
    nsv6780314copy number variation1nstd229human GRCh38 chr6: 11,700,911-11,705,073 , GRCh37.p13 chr6: 11,701,144-11,705,306 LOC340184
    nsv6409723copy number variation1nstd223human GRCh38 chr6: 7,366,072-12,459,745 , GRCh37.p13 chr6: 7,366,305-12,459,977 EEF1E1, RPS26P29, 82 more genes
    nsv6397457copy number variation1nstd223human GRCh38 chr6: 11,700,911-11,705,069 , GRCh37.p13 chr6: 11,701,144-11,705,302 LOC340184
    nsv6315320copy number variation1nstd102humanUncertain significance GRCh38 chr6: 11,481,309-12,522,879 , GRCh37.p13 chr6: 11,481,542-12,523,111 ADTRP, HIVEP1, 15 more genes
    nsv6135707copy number variation1nstd213human GRCh37 chr6: 11,010,000-11,730,001 , GRCh38.p12 chr6: 11,009,767-11,729,768 SMIM13, THAP12P5, 13 more genes
    nsv5087217mobile element insertion1nstd203human GRCh38 chr6: 11,700,585-11,700,601 , GRCh37.p13 chr6: 11,700,818-11,700,834 LOC340184
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4932725copy number variation1nstd200human GRCh38 chr6: 11,675,030-11,729,568 , GRCh37.p13 chr6: 11,675,263-11,729,801 , 2 more genes
    nsv4809727copy number variation1nstd200human GRCh37 chr6: 11,675,262-11,729,801 , GRCh38.p12 chr6: 11,675,029-11,729,568 , 2 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4324882inversion1nstd166human GRCh37.p13 chr6: 11,087,007-14,472,606 , GRCh38.p12 chr6: 11,086,774-14,472,375 , HIVEP1, 56 more genes
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