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Items: 1 to 20 of 91

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3118081copy number variation72nstd145human GRCh37 chr7: 141,766,533-141,793,377 , GRCh38.p12 chr7|NT_187562.1: 28,613-55,457 , GRCh38.p12 chr7: 142,066,733-142,093,577 MGAM
    nsv3117809copy number variation152nstd145human GRCh37 chr20: 1,561,593-1,584,273 , GRCh38.p12 chr20: 1,580,947-1,603,627 SIRPB1
    nsv3117855copy number variation14nstd145human GRCh37 chr19: 41,351,463-41,372,509 , GRCh38.p12 chr19: 40,845,558-40,866,604 CYP2A6
    nsv3117354copy number variation83nstd145human GRCh37 chr17: 15,043,995-15,058,468 , GRCh38.p12 chr17: 15,140,678-15,155,151 LOC107984976
    nsv3117451copy number variation18nstd145human GRCh37 chr6: 80,557,220-80,570,188 , GRCh38.p12 chr6: 79,847,503-79,860,471 LOC100422671
    nsv3115697copy number variation53nstd145human GRCh37 chr11: 7,814,824-7,826,930 , GRCh38.p12 chr11: 7,793,277-7,805,383 , GRCh38.p12 chr11|NT_187583.1: 14,145-26,251 , GRCh38.p12 chr11|NW_011332695.1: 14,145-26,251 OR5P2
    nsv3118025copy number variation35nstd145human GRCh37 chr8: 15,402,271-15,412,465 , GRCh38.p12 chr8: 15,544,762-15,554,956 TUSC3
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3117920copy number variation33nstd145human GRCh37 chr17: 50,117,130-50,126,228 , GRCh38.p12 chr17: 52,039,770-52,048,868 CA10
    nsv3112484copy number variation10nstd145human GRCh37 chr11: 55,434,547-55,443,378 , GRCh38.p12 chr11: 55,667,071-55,675,902 OR4V1P
    nsv3116281copy number variation19nstd145human GRCh37 chr3: 37,978,379-37,986,758 , GRCh38.p12 chr3: 37,936,888-37,945,267 CTDSPL
    nsv3116140copy number variation45nstd145human GRCh37 chr4: 21,369,066-21,376,838 , GRCh38.p12 chr4: 21,367,443-21,375,215 KCNIP4
    nsv3117799copy number variation1nstd145human GRCh37 chr8: 39,632,738-39,640,172 , GRCh38.p12 chr8: 39,775,219-39,782,653 , GRCh38.p12 chr8|NT_187577.1: 525,854-533,288 ADAM2
    nsv3114475copy number variation50nstd145human GRCh37 chr5: 12,811,448-12,818,768 , GRCh38.p12 chr5: 12,811,336-12,818,656 LOC105374657
    nsv3110514copy number variation75nstd145human GRCh37 chr8: 51,031,100-51,038,303 , GRCh38.p12 chr8: 50,118,540-50,125,743 SNTG1
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3110252copy number variation20nstd145human GRCh37 chr11: 55,445,882-55,451,346 , GRCh38.p12 chr11: 55,678,406-55,683,870 OR4P1P
    nsv3117711copy number variation27nstd145human GRCh37 chr3: 22,280,757-22,285,798 , GRCh38.p12 chr3: 22,239,265-22,244,306 ZNF385D
    nsv3117008copy number variation1nstd145human GRCh37 chr2: 55,019,629-55,024,507 , GRCh38.p12 chr2: 54,792,492-54,797,370 EML6
    nsv3113172copy number variation17nstd145human GRCh37 chr7: 112,515,072-112,519,782 , GRCh38.p12 chr7: 112,875,017-112,879,727 BMT2
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