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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7060683inversion1nstd229human GRCh38 chr8: 100,295,900-100,296,000 , GRCh37.p13 chr8: 101,308,128-101,308,228 RNF19A
    nsv6858022copy number variation1nstd229human GRCh38 chr8: 100,093,901-100,262,000 , GRCh37.p13 chr8: 101,106,129-101,274,228 UFM1P3, RNF19A, 5 more genes
    nsv6857665copy number variation1nstd229human GRCh38 chr8: 100,327,441-100,332,984 , GRCh37.p13 chr8: 101,339,669-101,345,212 RNF19A
    nsv6857193copy number variation1nstd229human GRCh38 chr8: 100,331,322-100,333,920 , GRCh37.p13 chr8: 101,343,550-101,346,148 RNF19A
    nsv6856264copy number variation1nstd229human GRCh38 chr8: 100,264,565-100,264,673 , GRCh37.p13 chr8: 101,276,793-101,276,901 RNF19A
    nsv6852354copy number variation1nstd229human GRCh38 chr8: 100,303,301-100,357,300 , GRCh37.p13 chr8: 101,315,529-101,369,528 RNF19A
    nsv6848142copy number variation1nstd229human GRCh38 chr8: 100,324,801-100,512,600 , GRCh37.p13 chr8: 101,337,029-101,524,828 MIR4471, LOC105375670, 2 more genes
    nsv6847395copy number variation1nstd229human GRCh38 chr8: 100,007,701-100,261,900 , GRCh37.p13 chr8: 101,019,929-101,274,128 UFM1P3, RNF19A, 5 more genes
    nsv6845975copy number variation1nstd229human GRCh38 chr8: 100,252,902-100,256,150 , GRCh37.p13 chr8: 101,265,130-101,268,378 RNF19A
    nsv6843879copy number variation1nstd229human GRCh38 chr8: 100,316,596-100,318,971 , GRCh37.p13 chr8: 101,328,824-101,331,199 RNF19A
    nsv6839151copy number variation1nstd229human GRCh38 chr8: 100,309,141-100,309,171 , GRCh37.p13 chr8: 101,321,369-101,321,399 RNF19A
    nsv6637993copy number variation1nstd102humanUncertain significance GRCh37 chr8: 100,791,384-101,278,033 , GRCh38.p12 chr8: 99,779,156-100,265,805 RNF19A, POLR2K, 8 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6571016inversion1nstd223human GRCh38 chr8: 100,303,709-100,304,062 , GRCh37.p13 chr8: 101,315,937-101,316,290 RNF19A
    nsv6431163copy number variation1nstd223human GRCh38 chr8: 100,310,601-100,317,700 , GRCh37.p13 chr8: 101,322,829-101,329,928 RNF19A
    nsv6428773copy number variation1nstd223human GRCh38 chr8: 100,296,501-100,298,800 , GRCh37.p13 chr8: 101,308,729-101,311,028 RNF19A
    nsv6428349copy number variation1nstd223human GRCh38 chr8: 100,324,379-100,365,762 , GRCh37.p13 chr8: 101,336,607-101,377,990 RNF19A
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