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Items: 10

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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6627347copy number variation1nstd224human GRCh37 chr2: 144,193,257-144,290,246 , GRCh38.p12 chr2: 143,435,688-143,532,677 ARHGAP15
    nsv6629980copy number variation4nstd224human GRCh37 chr4: 71,566-87,277 , GRCh38.p12 chr4: 71,674-87,387 ZNF595
    nsv6624585copy number variation1nstd224human GRCh37 chr18: 29,410,750-29,470,718 , GRCh38.p12 chr18: 31,830,787-31,890,755 TRAPPC8, LOC100421591
    nsv6629371copy number variation12nstd224human GRCh37 chr4: 144,994,903-145,038,131 , GRCh38.p12 chr4: 144,073,750-144,116,978 GYPA, LOC105377460
    nsv6624844copy number variation645nstd224human GRCh37 chr19: 20,630,360-20,715,228 , GRCh38.p12 chr19: 20,447,554-20,532,422 ZNF737, LOC105372316, 1 more genes
    nsv6622775copy number variation50nstd224human GRCh37 chr15: 20,161,372-20,192,086 , GRCh38.p12 chr15: 19,956,119-19,986,833 IGHV1OR15-9, SLC20A1P3, 1 more genes
    nsv6624790copy number variation10nstd224human GRCh37 chr19: 53,932,295-53,997,114 , GRCh38.p12 chr19: 53,429,042-53,493,860 ZNF813, TPM3P9, 5 more genes
    nsv6620265copy number variation201nstd224human GRCh37 chr10: 135,256,762-135,379,710 , GRCh38.p12 chr10: 133,443,258-133,566,206 CYP2E1, OR7M1P, 4 more genes
    nsv6622955copy number variation54nstd224human GRCh37 chr15: 22,368,588-22,468,503 , GRCh38.p12 chr15: 22,080,637-22,180,552 OR4N4, RPS8P10, 6 more genes
    nsv6632147copy number variation132nstd224human GRCh37 chr7: 44,935-67,365 , GRCh38.p12 chr7: 44,935-67,365 , GRCh38.p12 chr7|NT_187558.1: 1,034-23,464 , GRCh38.p12 chr7|NT_187653.1: 37,256-59,686 0
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