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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099185copy number variation1nstd231human GRCh38.p12 chr1: 23,256,354-23,442,990 , GRCh37 chr1: 23,582,847-23,769,483 , GRCh38.p12 chr1|NW_014040926.1: 47,042-212,969 TCEA3, HNRNPR, 4 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7044760inversion1nstd229human GRCh38 chr1: 22,155,852-26,348,296 , GRCh37.p13 chr1: 22,482,345-26,674,787 MIR4684, PDIK1L, 120 more genes
    nsv6647483copy number variation1nstd229human GRCh38 chr1: 23,337,278-23,337,447 , GRCh37.p13 chr1: 23,663,771-23,663,940 HNRNPR
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6543442inversion1nstd223human GRCh38 chr1: 23,332,687-23,334,093 , GRCh37.p13 chr1: 23,659,180-23,660,586 HNRNPR
    nsv6542002inversion1nstd223human GRCh38 chr1: 23,334,924-23,336,043 , GRCh37.p13 chr1: 23,661,417-23,662,536 HNRNPR
    nsv6334173copy number variation1nstd223human GRCh38 chr1: 23,324,968-23,330,332 , GRCh37.p13 chr1: 23,651,461-23,656,825 HNRNPR
    nsv6328301copy number variation1nstd223human GRCh38 chr1: 23,308,279-23,308,793 , GRCh37.p13 chr1: 23,634,772-23,635,286 HNRNPR
    nsv6326976copy number variation1nstd223human GRCh38 chr1: 23,312,439-23,313,061 , GRCh37.p13 chr1: 23,638,932-23,639,554 HNRNPR
    nsv6326352copy number variation1nstd223human GRCh38 chr1: 23,307,818-23,308,630 , GRCh37.p13 chr1: 23,634,311-23,635,123 HNRNPR
    nsv6325976copy number variation1nstd223human GRCh38 chr1: 23,308,988-23,309,534 , GRCh37.p13 chr1: 23,635,481-23,636,027 HNRNPR
    nsv6322367copy number variation1nstd223human GRCh38 chr1: 23,304,601-23,306,000 , GRCh37.p13 chr1: 23,631,094-23,632,493 HNRNPR
    nsv6319725copy number variation1nstd223human GRCh38 chr1: 23,343,301-23,346,200 , GRCh37.p13 chr1: 23,669,794-23,672,693 HNRNPR
    nsv6318055copy number variation1nstd223human GRCh38 chr1: 23,307,430-23,308,221 , GRCh37.p13 chr1: 23,633,923-23,634,714 HNRNPR
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv6133572copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,950,001 , GRCh38.p12 chr1: 16,943,505-26,623,510 ALPL, C1QA, 250 more genes
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