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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884551copy number variation1nstd102humanLikely benign GRCh37 chr3: 62,477,896-62,799,740 , GRCh38.p12 chr3: 62,492,221-62,814,065 CADPS, RPL14P2, 2 more genes
    nsv3891395copy number variation1nstd102humanBenign GRCh37 chr12: 63,334,956-63,455,304 , GRCh38.p12 chr12: 62,941,176-63,061,524 LDHAL6CP, RPL14P1, 2 more genes
    nsv3908582copy number variation1nstd102humanBenign GRCh37 chr12: 95,467,354-95,548,473 , GRCh38.p12 chr12: 95,073,578-95,154,697 FGD6, RPL14P4, 2 more genes
    nsv6291596copy number variation1nstd102humanUncertain significance GRCh37 chr12: 95,475,366-95,601,325 , GRCh38.p12 chr12: 95,081,590-95,207,549 RPL14P4, FGD6, 1 more genes
    nsv6290814copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,722,354-62,971,421 , GRCh38.p12 chr3: 62,736,679-62,985,746 RPS10P10, CADPS, 3 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3917126copy number variation1nstd102humanPathogenic GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052 SETD7, HSPD1P5, 294 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 RPL14, LOC102724104, 291 more genes
    nsv3874323copy number variation1nstd102humanPathogenic GRCh37 chr4: 126,549,693-141,313,049 , GRCh38.p12 chr4: 125,628,538-140,391,895 FTH1P24, SNHG27, 127 more genes
    nsv3912421copy number variation1nstd102humanPathogenic NCBI36 chr4: 129,260,477-143,571,978 , GRCh37 chr4: 129,041,027-143,352,528 , GRCh38 chr4: 128,119,872-142,431,375 PCDH10-DT, RNU6-1214P, 120 more genes
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 MAGI1-AS1, FEZF2, 135 more genes
    nsv6290933copy number variation1nstd102humanPathogenic GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004 NDUFB4P1, UBA3, 110 more genes
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv6291168copy number variation1nstd102humanPathogenic GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146 LOC105377447, RN7SKP253, 92 more genes
    nsv3917204copy number variation1nstd102humanPathogenic GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197 C3orf49, PPIAP16, 93 more genes
    nsv4674499copy number variation1nstd102humanPathogenic GRCh37 chr4: 139,531,815-146,095,109 , GRCh38.p12 chr4: 138,610,661-145,173,957 GUSBP5, LOC100287014, 77 more genes
    nsv3922383copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,956,521-68,514,983 , NCBI36 chr3: 61,931,561-68,597,673 , GRCh38 chr3: 61,970,847-68,465,832 UBL5P3, PRICKLE2-DT, 73 more genes
    nsv3911302copy number variation1nstd102humanPathogenic GRCh38 chr12: 57,013,355-63,042,498 , NCBI36 chr12: 55,693,406-61,722,545 , GRCh37 chr12: 57,407,139-63,436,278 CTDSP2, LINC01465, 97 more genes
    nsv3916302copy number variation1nstd102humanPathogenic NCBI36 chr12: 59,587,199-65,248,124 , GRCh37 chr12: 61,300,932-66,961,857 , GRCh38 chr12: 60,907,151-66,568,077 LOC105369809, SRGAP1, 93 more genes
    nsv4674306copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,449,667-65,561,638 , GRCh38.p12 chr3: 60,463,934-65,575,963 THOC7-AS1, LOC105377647, 56 more genes
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