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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3117955copy number variation13nstd145human GRCh37 chr19: 41,351,463-41,379,048 , GRCh38.p12 chr19: 40,845,558-40,873,143 CYP2A6
    nsv3115762copy number variation5nstd145human GRCh37 chr7: 141,766,533-141,792,941 , GRCh38.p12 chr7: 142,066,733-142,093,141 , GRCh38.p12 chr7|NT_187562.1: 28,613-55,021 MGAM
    nsv3113269copy number variation34nstd145human GRCh37 chr20: 1,558,341-1,584,273 , GRCh38.p12 chr20: 1,577,695-1,603,627 SIRPB1
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111851copy number variation1nstd145human GRCh37 chr19: 29,775,069-29,785,468 , GRCh38.p12 chr19: 29,284,162-29,294,561 VSTM2B-DT
    nsv3118340copy number variation1nstd145human GRCh37 chr1: 17,853,751-17,862,547 , GRCh38.p12 chr1: 17,527,255-17,536,052 ARHGEF10L
    nsv3111360copy number variation20nstd145human GRCh37 chr14: 80,106,745-80,114,965 , GRCh38.p12 chr14: 79,640,402-79,648,622 NRXN3
    nsv3110883copy number variation1nstd145human GRCh37 chr19: 18,134,973-18,142,063 , GRCh38.p12 chr19: 18,024,164-18,031,253 CSP3
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3112029copy number variation8nstd145human GRCh37 chr15: 29,901,945-29,908,247 , GRCh38.p12 chr15|NW_011332701.1: 1,781,378-1,787,680 , GRCh38.p12 chr15: 29,609,741-29,616,043 , GRCh38.p12 chr15|NT_187660.1: 1,893,862-1,900,164 TUBBP8
    nsv3113323copy number variation1nstd145human GRCh37 chr17: 71,186,724-71,192,700 , GRCh38.p12 chr17: 73,190,585-73,196,561 COG1
    nsv3116197copy number variation63nstd145human GRCh37 chr7: 151,606-157,474 , GRCh38.p12 chr7: 151,606-157,474 , GRCh38.p12 chr7|NT_187558.1: 107,411-113,280 , GRCh38.p12 chr7|NT_187653.1: 143,927-149,795 LINC03014
    nsv3110559copy number variation79nstd145human GRCh37 chr2: 49,534,030-49,539,079 , GRCh38.p12 chr2: 49,306,891-49,311,940 LOC105374595
    nsv3113205copy number variation26nstd145human GRCh37 chr3: 131,708,215-131,712,626 , GRCh38.p12 chr3: 131,989,371-131,993,782 CPNE4
    nsv3112046copy number variation55nstd145human GRCh37 chr19: 54,556,015-54,560,055 , GRCh38.p12 chr19: 54,052,761-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571061.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571057.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571058.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571059.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571060.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571056.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571055.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571054.1: 27,128-31,168 VSTM1
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
    nsv3113770copy number variation1nstd145human GRCh37 chr8: 97,261,626-97,264,784 , GRCh38.p12 chr8: 96,249,398-96,252,556 MTERF3
    nsv3114073copy number variation1nstd145human GRCh37 chr15: 97,629,484-97,632,604 , GRCh38.p12 chr15: 97,086,254-97,089,374 LOC105371004
    nsv3112503copy number variation1nstd145human GRCh37 chr8: 3,119,772-3,122,846 , GRCh38.p12 chr8: 3,262,250-3,265,324 CSMD1
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