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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4368270copy number variation1nstd173human GRCh37 chr13: 106,223,313-106,309,859 , GRCh38.p12 chr13: 105,570,964-105,657,510 LOC105370345
    nsv4380190copy number variation32nstd173human GRCh37 chr2: 98,079,569-98,162,176 , GRCh38.p12 chr2: 97,490,656-97,545,713 ANKRD36B
    nsv4385823copy number variation12nstd173human GRCh37 chr15: 34,929,751-34,977,813 , GRCh38.p12 chr15: 34,637,550-34,685,612 LINC02252
    nsv4379349copy number variation357nstd173human GRCh37 chr20: 1,560,549-1,597,997 , GRCh38.p12 chr20: 1,579,903-1,617,351 SIRPB1
    nsv4375449copy number variation2nstd173human GRCh37 chr2: 194,568,100-194,601,354 , GRCh38.p12 chr2: 193,703,376-193,736,630 SEC61GP1
    nsv4375488copy number variation51nstd173human GRCh37 chr1: 196,714,810-196,741,354 , GRCh38.p12 chr1: 196,745,680-196,772,224 CFH
    nsv4373972copy number variation1nstd173human GRCh37 chr10: 133,499,053-133,634,968 , GRCh38.p12 chr10: 131,666,717-131,802,632 LINC01164
    nsv4366884copy number variation20nstd173human GRCh37 chr3: 173,239,853-173,300,050 , GRCh38.p12 chr3: 173,522,063-173,582,260 NLGN1
    nsv4370174copy number variation1nstd173human GRCh37 chr7: 146,226,419-146,254,889 , GRCh38.p12 chr7: 146,529,327-146,557,797 CNTNAP2
    nsv4376456copy number variation1782nstd173human GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445 ADAM5, ADAM3A
    nsv4387915copy number variation2nstd173human GRCh37 chr6: 95,982,530-96,071,088 , GRCh38.p12 chr6: 95,534,654-95,623,212 MANEA-DT, MANEA
    nsv4367571copy number variation18nstd173human GRCh37 chr12: 11,496,808-11,553,849 , GRCh38.p12 chr12: 11,343,874-11,400,915 , GRCh38.p12 chr12|NT_187658.1: 538,837-572,349 PRB1, PRB2
    nsv4370464copy number variation362nstd173human GRCh37 chr11: 4,967,239-4,991,060 , GRCh38.p12 chr11: 4,946,009-4,969,830 OR51A4, OR51A2
    nsv4373867copy number variation1nstd173human GRCh37 chr19: 51,154,040-51,174,751 , GRCh38.p12 chr19: 50,650,783-50,671,494 SHANK1, C19orf81
    nsv4385636copy number variation51nstd173human GRCh37 chr2: 13,202,931-13,279,945 , GRCh38.p12 chr2: 13,062,806-13,139,820 LOC105373436, LOC105373484
    nsv4384457copy number variation635nstd173human GRCh37 chr11: 55,374,031-55,453,008 , GRCh38.p12 chr11: 55,606,555-55,685,532 OR4P1P, OR4C6, 3 more genes
    nsv4375116copy number variation12nstd173human GRCh37 chr11: 134,348,704-134,719,852 , GRCh38.p12 chr11: 134,478,810-134,849,958 LINC02706, B3GAT1-DT, 2 more genes
    nsv4382508copy number variation18nstd173human GRCh37 chr16: 15,054,346-15,126,890 , GRCh38.p12 chr16: 14,960,489-15,033,033 MIR1972-1, LOC728138, 1 more genes
    nsv4366127copy number variation5nstd173human GRCh37 chr5: 180,381,989-180,442,428 , GRCh38.p12 chr5: 180,954,989-181,015,428 BTNL3, RNU6-1036P, 3 more genes
    nsv4380515copy number variation77nstd173human GRCh37 chr12: 8,558,475-8,594,982 , GRCh38.p12 chr12: 8,405,879-8,442,386 OR7E148P, OR7E149P, 1 more genes
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