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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111623copy number variation16nstd145human GRCh37 chr5: 41,232,035-41,243,881 , GRCh38.p12 chr5: 41,231,933-41,243,779 C6
    nsv3114301copy number variation2nstd145human GRCh37 chr14: 49,408,611-49,420,165 , GRCh38.p12 chr14: 48,939,408-48,950,962 LOC105378178
    nsv3110942copy number variation60nstd145human GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181 LINC02932
    nsv3116948copy number variation9nstd145human GRCh37 chr11: 55,434,691-55,443,378 , GRCh38.p12 chr11: 55,667,215-55,675,902 OR4V1P
    nsv3111360copy number variation20nstd145human GRCh37 chr14: 80,106,745-80,114,965 , GRCh38.p12 chr14: 79,640,402-79,648,622 NRXN3
    nsv3111031copy number variation3nstd145human GRCh37 chr15: 48,207,720-48,215,361 , GRCh38.p12 chr15: 47,915,523-47,923,164 LOC105370805
    nsv3117297copy number variation80nstd145human GRCh37 chr7: 154,392,836-154,399,317 , GRCh38.p12 chr7: 154,601,126-154,607,607 DPP6
    nsv3112895copy number variation76nstd145human GRCh37 chr12: 43,020,941-43,027,293 , GRCh38.p12 chr12: 42,627,139-42,633,491 LINC02402
    nsv3110559copy number variation79nstd145human GRCh37 chr2: 49,534,030-49,539,079 , GRCh38.p12 chr2: 49,306,891-49,311,940 LOC105374595
    nsv3114222copy number variation54nstd145human GRCh37 chr12: 82,139,806-82,144,215 , GRCh38.p12 chr12: 81,746,027-81,750,436 PPFIA2
    nsv3113902copy number variation1nstd145human GRCh37 chr4: 62,718,601-62,722,967 , GRCh38.p12 chr4: 61,852,883-61,857,249 ADGRL3
    nsv3116880copy number variation32nstd145human GRCh37 chr6: 101,934,608-101,938,909 , GRCh38.p12 chr6: 101,486,732-101,491,033 GRIK2
    nsv3111683copy number variation4nstd145human GRCh37 chr5: 115,389,300-115,393,543 , GRCh38.p12 chr5: 116,053,603-116,057,846 ARL14EPL
    nsv3117950copy number variation1nstd145human GRCh37 chr4: 12,946,827-12,951,028 , GRCh38.p12 chr4: 12,945,203-12,949,404 LOC105374493
    nsv3115927copy number variation2nstd145human GRCh37 chr5: 85,645,180-85,649,277 , GRCh38.p12 chr5: 86,349,362-86,353,459 LOC105379064
    nsv3114451copy number variation90nstd145human GRCh37 chr12: 90,487,994-90,491,654 , GRCh38.p12 chr12: 90,094,217-90,097,877 LOC105369890
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
    nsv3115059copy number variation18nstd145human GRCh37 chr1: 62,113,512-62,116,470 , GRCh38.p12 chr1: 61,647,840-61,650,798 LOC107984964
    nsv3117776copy number variation27nstd145human GRCh37 chr9: 20,801,780-20,804,551 , GRCh38.p12 chr9: 20,801,781-20,804,552 FOCAD
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