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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7098903copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,964,745-22,385,630 , GRCh38.p12 chr16: 21,953,424-22,374,309 , GRCh38.p12 chr16|NW_017852933.1: 730,730-1,151,615 CDR2, UQCRC2, 12 more genes
    nsv7093405copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,780,595-22,385,630 , GRCh38.p12 chr16: 21,769,274-22,374,309 , GRCh38.p12 chr16|NW_017852933.1: 730,730-1,335,506 CDR2, UQCRC2, 19 more genes
    nsv7093393copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 21,846,039-22,385,630 , GRCh38.p12 chr16: 21,834,718-22,374,309 , GRCh38.p12 chr16|NW_017852933.1: 730,730-1,270,057 CDR2, UQCRC2, 17 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7067843inversion1nstd229human GRCh38 chr16: 21,291,198-22,687,975 , GRCh37.p13 chr16: 21,302,519-22,699,296 SMG1P4, NPIPB5, 41 more genes
    nsv7066172inversion1nstd229human GRCh38 chr16: 21,576,182-22,802,537 , GRCh37.p13 chr16: 21,587,503-22,813,858 UQCRC2, VWA3A, 31 more genes
    nsv7062907inversion1nstd229human GRCh38 chr16: 21,501,792-22,437,451 , GRCh37.p13 chr16: 21,513,113-22,448,772 LOC100420536, RRN3P3, 31 more genes
    nsv7060613inversion1nstd229human GRCh38 chr16: 21,590,269-22,770,847 , GRCh37.p13 chr16: 21,601,590-22,782,168 LOC105371129, OTOAP1, 31 more genes
    nsv7060602inversion1nstd229human GRCh38 chr16: 22,087,809-24,116,610 , GRCh37.p13 chr16: 22,099,130-24,127,931 RRN3P3, MFSD13B, 34 more genes
    nsv7058720inversion1nstd229human GRCh38 chr16: 21,529,628-23,453,946 , GRCh37.p13 chr16: 21,540,949-23,465,267 CDR2-DT, LOC105371131, 40 more genes
    nsv7058493inversion1nstd229human GRCh38 chr16: 21,334,980-22,395,842 , GRCh37.p13 chr16: 21,346,301-22,407,163 LOC101927814, METTL9, 32 more genes
    nsv6994087copy number variation1nstd229human GRCh38 chr16: 22,361,904-22,375,136 , GRCh37.p13 chr16: 22,373,225-22,386,457 CDR2-DT, CDR2
    nsv6985872copy number variation1nstd229human GRCh38 chr16: 22,346,907-22,414,695 , GRCh37.p13 chr16: 22,358,228-22,426,016 MFSD13B, CDR2-DT, 1 more genes
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6637228copy number variation1nstd102humanUncertain significance GRCh37 chr16: 21,967,066-22,431,357 , GRCh38.p12 chr16: 21,955,745-22,420,036 , GRCh38.p12 chr16|NW_017852933.1: 685,003-1,149,293 CDR2, EEF2K, 14 more genes
    nsv6635014copy number variation1nstd227human GRCh38.p12 chr16: 21,937,801-22,398,142 , GRCh37 chr16: 21,949,122-22,409,463 , GRCh38.p12 chr16|NW_017852933.1: 706,897-1,167,239 CDR2, UQCRC2, 14 more genes
    nsv6623427copy number variation2nstd224human GRCh37 chr16: 21,966,869-22,392,905 , GRCh38.p12 chr16: 21,955,548-22,381,584 , GRCh38.p12 chr16|NW_017852933.1: 723,455-1,149,490 EEF2K, POLR3E, 12 more genes
    nsv6623426copy number variation1nstd224human GRCh37 chr16: 21,811,499-22,435,843 , GRCh38.p12 chr16: 21,800,178-22,424,522 , GRCh38.p12 chr16|NW_017852933.1: 680,517-1,304,603 EEF2K, POLR3E, 20 more genes
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