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Items: 1 to 20 of 386

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147676copy number variation1nstd232human GRCh37.p13 chr2: 29,228,497-29,228,565 , GRCh38.p12 chr2: 29,005,631-29,005,699 TOGARAM2
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7049166inversion1nstd229human GRCh38 chr2: 29,020,409-29,020,471 , GRCh37.p13 chr2: 29,243,275-29,243,337 TOGARAM2
    nsv7045006inversion1nstd229human GRCh38 chr2: 28,892,565-29,348,187 , GRCh37.p13 chr2: 29,115,431-29,571,053 SNORD92, LOC105374386, 8 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv6674081copy number variation1nstd229human GRCh38 chr2: 29,023,055-29,042,916 , GRCh37.p13 chr2: 29,245,921-29,265,782 TOGARAM2
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6672564copy number variation1nstd229human GRCh38 chr2: 29,002,731-29,006,589 , GRCh37.p13 chr2: 29,225,597-29,229,455 TOGARAM2
    nsv6672552copy number variation1nstd229human GRCh38 chr2: 28,992,785-28,995,225 , GRCh37.p13 chr2: 29,215,651-29,218,091 TOGARAM2
    nsv6669610copy number variation1nstd229human GRCh38 chr2: 28,986,707-28,991,799 , GRCh37.p13 chr2: 29,209,573-29,214,665 TOGARAM2
    nsv6669588copy number variation1nstd229human GRCh38 chr2: 28,984,910-28,989,648 , GRCh37.p13 chr2: 29,207,776-29,212,514 TOGARAM2
    nsv6666609copy number variation1nstd229human GRCh38 chr2: 29,050,800-29,059,118 , GRCh37.p13 chr2: 29,273,666-29,281,984 TOGARAM2
    nsv6665994copy number variation1nstd229human GRCh38 chr2: 28,736,946-29,025,229 , GRCh37.p13 chr2: 28,959,812-29,248,095 TOGARAM2, PPP1CB-DT, 7 more genes
    nsv6664502copy number variation1nstd229human GRCh38 chr2: 29,009,977-29,013,710 , GRCh37.p13 chr2: 29,232,843-29,236,576 TOGARAM2
    nsv6664351copy number variation1nstd229human GRCh38 chr2: 28,985,105-28,989,653 , GRCh37.p13 chr2: 29,207,971-29,212,519 TOGARAM2
    nsv6663628copy number variation1nstd229human GRCh38 chr2: 29,021,500-29,021,566 , GRCh37.p13 chr2: 29,244,366-29,244,432 TOGARAM2
    nsv6662778copy number variation1nstd229human GRCh38 chr2: 28,991,051-29,003,665 , GRCh37.p13 chr2: 29,213,917-29,226,531 TOGARAM2
    nsv6661015copy number variation1nstd229human GRCh38 chr2: 28,976,767-28,980,556 , GRCh37.p13 chr2: 29,199,633-29,203,422 TOGARAM2
    nsv6660802copy number variation1nstd229human GRCh38 chr2: 29,052,001-29,058,100 , GRCh37.p13 chr2: 29,274,867-29,280,966 TOGARAM2
    nsv6660291copy number variation1nstd229human GRCh38 chr2: 29,029,022-29,029,145 , GRCh37.p13 chr2: 29,251,888-29,252,011 TOGARAM2
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