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Items: 1 to 20 of 265

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145477copy number variation1nstd232human GRCh37.p13 chr16: 23,419,653-23,419,720 , GRCh38.p12 chr16: 23,408,332-23,408,399 COG7
    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
    nsv7094827copy number variation1nstd102humanUncertain significance GRCh37 chr16: 23,193,865-23,652,612 , GRCh38.p12 chr16: 23,182,544-23,641,291 PALB2, SCNN1G, 10 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
    nsv6995628copy number variation1nstd229human GRCh38 chr16: 23,419,275-23,428,042 , GRCh37.p13 chr16: 23,430,596-23,439,363 COG7
    nsv6995391copy number variation1nstd229human GRCh38 chr16: 23,334,773-23,534,768 , GRCh37.p13 chr16: 23,346,094-23,546,089 COG7, RN7SKP23, 4 more genes
    nsv6988694copy number variation1nstd229human GRCh38 chr16: 23,422,282-23,428,776 , GRCh37.p13 chr16: 23,433,603-23,440,097 COG7
    nsv6987594copy number variation1nstd229human GRCh38 chr16: 23,451,879-23,553,770 , GRCh37.p13 chr16: 23,463,200-23,565,091 GGA2, EARS2, 3 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
    nsv6589777inversion1nstd223human GRCh38 chr16: 23,447,467-23,447,716 , GRCh37.p13 chr16: 23,458,788-23,459,037 COG7
    nsv6584180inversion1nstd223human GRCh38 chr16: 23,393,783-23,394,975 , GRCh37.p13 chr16: 23,405,104-23,406,296 COG7
    nsv6500893copy number variation1nstd223human GRCh38 chr16: 23,334,773-23,534,770 , GRCh37.p13 chr16: 23,346,094-23,546,091 COG7, RN7SKP23, 4 more genes
    nsv6309663copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,464,127-23,635,435 , GRCh38.p12 chr16: 23,452,806-23,624,114 NDUFAB1, GGA2, 6 more genes
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6197378copy number variation1nstd214human GRCh38 chr16: 23,408,332-23,408,399 , GRCh37.p13 chr16: 23,419,653-23,419,720 COG7
    nsv6133270copy number variation1nstd213human GRCh37 chr16: 23,390,000-23,530,001 , GRCh38.p12 chr16: 23,378,679-23,518,680 SCNN1B, GGA2, 3 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
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