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Items: 1 to 20 of 474

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095856copy number variation1nstd102humanUncertain significance GRCh37 chr2: 135,809,878-136,875,630 , GRCh38.p12 chr2: 135,052,308-136,118,060 G3BP1P1, UBXN4, 14 more genes
    nsv7053909inversion1nstd229human GRCh38 chr2: 135,710,529-135,746,014 , GRCh37.p13 chr2: 136,468,099-136,503,584 R3HDM1, LOC107985946, 1 more genes
    nsv7052866inversion1nstd229human GRCh38 chr2: 135,715,809-135,715,922 , GRCh37.p13 chr2: 136,473,379-136,473,492 R3HDM1
    nsv6693148copy number variation1nstd229human GRCh38 chr2: 135,645,133-135,645,211 , GRCh37.p13 chr2: 136,402,703-136,402,781 R3HDM1
    nsv6692956copy number variation1nstd229human GRCh38 chr2: 135,691,966-135,707,859 , GRCh37.p13 chr2: 136,449,536-136,465,429 R3HDM1
    nsv6692775copy number variation1nstd229human GRCh38 chr2: 135,625,001-135,859,100 , GRCh37.p13 chr2: 136,382,571-136,616,670 LCT-AS1, RNU6-512P, 6 more genes
    nsv6692713copy number variation1nstd229human GRCh38 chr2: 135,563,601-135,568,000 , GRCh37.p13 chr2: 136,321,171-136,325,570 R3HDM1
    nsv6692079copy number variation1nstd229human GRCh38 chr2: 135,590,165-135,597,456 , GRCh37.p13 chr2: 136,347,735-136,355,026 R3HDM1
    nsv6691721copy number variation1nstd229human GRCh38 chr2: 135,536,201-135,541,900 , GRCh37.p13 chr2: 136,293,771-136,299,470 R3HDM1
    nsv6690257copy number variation1nstd229human GRCh38 chr2: 135,699,181-135,699,253 , GRCh37.p13 chr2: 136,456,751-136,456,823 R3HDM1
    nsv6689335copy number variation1nstd229human GRCh38 chr2: 135,722,653-135,722,779 , GRCh37.p13 chr2: 136,480,223-136,480,349 R3HDM1
    nsv6685506copy number variation1nstd229human GRCh38 chr2: 135,492,767-135,646,566 , GRCh37.p13 chr2: 136,250,337-136,404,136 R3HDM1, ZRANB3, 1 more genes
    nsv6685009copy number variation1nstd229human GRCh38 chr2: 135,546,629-135,550,019 , GRCh37.p13 chr2: 136,304,199-136,307,589 R3HDM1
    nsv6681979copy number variation1nstd229human GRCh38 chr2: 135,535,564-135,539,092 , GRCh37.p13 chr2: 136,293,134-136,296,662 R3HDM1
    nsv6681368copy number variation1nstd229human GRCh38 chr2: 135,682,223-135,688,908 , GRCh37.p13 chr2: 136,439,793-136,446,478 R3HDM1
    nsv6679692copy number variation1nstd229human GRCh38 chr2: 128,625,642-138,426,614 , GRCh37.p13 chr2: 129,383,216-139,184,184 MTND4P27, LOC646674, 194 more genes
    nsv6627760copy number variation1nstd224human GRCh37 chr2: 136,399,355-136,558,293 , GRCh38.p12 chr2: 135,641,785-135,800,723 LCT, UBXN4, 4 more genes
    nsv6627339copy number variation1nstd224human GRCh37 chr2: 135,699,619-136,374,311 , GRCh38.p12 chr2: 134,942,049-135,616,741 CCNT2, RAB3GAP1, 5 more genes
    nsv6627258copy number variation1nstd224human GRCh37 chr2: 136,279,157-136,403,272 , GRCh38.p12 chr2: 135,521,587-135,645,702 R3HDM1, ZRANB3
    nsv6555393inversion1nstd223human GRCh38 chr2: 135,697,959-135,698,239 , GRCh37.p13 chr2: 136,455,529-136,455,809 R3HDM1
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