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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3110960copy number variation10nstd145human GRCh37 chr4: 69,435,444-69,456,801 , GRCh38.p12 chr4: 68,569,726-68,591,083 UGT2B17
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3116724copy number variation1nstd145human GRCh37 chr1: 62,112,915-62,116,470 , GRCh38.p12 chr1: 61,647,243-61,650,798 LOC107984964
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
    nsv3112483copy number variation7nstd145human GRCh37 chr10: 3,628,328-3,631,250 , GRCh38.p12 chr10: 3,586,136-3,589,058 LOC105376360
    nsv3115311copy number variation23nstd145human GRCh37 chr3: 189,737,302-189,740,185 , GRCh38.p12 chr3: 190,019,513-190,022,396 P3H2
    nsv3115215copy number variation2nstd145human GRCh37 chr5: 167,059,246-167,061,975 , GRCh38.p12 chr5: 167,632,241-167,634,970 TENM2
    nsv3114933copy number variation1nstd145human GRCh37 chr19: 44,951,947-44,954,247 , GRCh38.p12 chr19: 44,447,759-44,450,059 ZNF229
    nsv3111015copy number variation7nstd145human GRCh37 chr7: 148,074,116-148,075,734 , GRCh38.p12 chr7: 148,377,024-148,378,642 CNTNAP2
    nsv3117482copy number variation8nstd145human GRCh37 chr4: 12,122,813-12,124,330 , GRCh38.p12 chr4: 12,121,189-12,122,706
    nsv3114312copy number variation223nstd145human GRCh37 chr2: 76,773,866-76,775,310 , GRCh38.p12 chr2: 76,546,740-76,548,184 LOC105374814
    nsv3110522copy number variation1nstd145human GRCh37 chr21: 44,970,847-44,983,016 , GRCh38.p12 chr21: 43,550,966-43,563,135 HSF2BP, RPL31P1
    nsv3112671copy number variation3nstd145human GRCh37 chr1: 245,439,735-245,442,330 , GRCh38.p12 chr1: 245,276,433-245,279,028 KIF26B, DNAJC19P8
    nsv3115370copy number variation11nstd145human GRCh37 chr17: 39,423,611-39,433,198 , GRCh38.p12 chr17: 41,267,359-41,276,946 , GRCh38.p12 chr17|NW_003871093.1: 30,164-39,751 KRTAP9-11P, KRTAP9-7, 1 more genes
    nsv3110903copy number variation122nstd145human GRCh37 chr2: 52,749,700-52,784,734 , GRCh38.p12 chr2: 52,522,562-52,557,596 0
    nsv3116586copy number variation8nstd145human GRCh37 chr4: 10,211,418-10,234,173 , GRCh38.p12 chr4: 10,209,794-10,232,549 0
    nsv3115280copy number variation32nstd145human GRCh37 chr4: 64,696,792-64,713,619 , GRCh38.p12 chr4: 63,831,074-63,847,901 0
    nsv3111954copy number variation25nstd145human GRCh37 chr5: 150,212,948-150,220,971 , GRCh38.p12 chr5: 150,833,386-150,841,409 0
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