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Items: 1 to 20 of 38004

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6137731copy number variation1nstd102humanBenign GRCh37 chrX: 1,412,907-1,412,990 , GRCh38 chrX: 1,294,014-1,294,097 , GRCh38 chrY: 1,294,014-1,294,097 , GRCh37 chrY: 1,362,907-1,362,990 CSF2RA, MIR3690
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6131470insertion1nstd186human GRCh37 chr19: 41,849,848-41,849,872 , GRCh38.p12 chr19: 41,343,943-41,343,967 TGFB1
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130675insertion1nstd186human GRCh37 chr20: 55,793,971-55,793,971 , GRCh38.p12 chr20: 57,218,915-57,218,915 BMP7
    nsv6129069copy number variation1nstd186human GRCh37 chr17: 4,640,607-4,641,461 , GRCh38.p12 chr17: 4,737,312-4,738,166 ZMYND15, CXCL16
    nsv6129029insertion1nstd186human GRCh37 chrX: 69,054,933-69,054,984 , GRCh38.p12 chrX: 69,835,089-69,835,140 EDA
    nsv6128074insertion1nstd186human GRCh37 chrX: 1,389,811-1,389,811 , GRCh38.p12 chrX: 1,270,918-1,270,918 CSF2RA
    nsv6127613insertion1nstd186human GRCh37 chrX: 1,413,967-1,413,967 , GRCh38.p12 chrX: 1,295,074-1,295,074 CSF2RA
    nsv6126512copy number variation1nstd186human GRCh37 chr21: 34,694,798-34,695,297 , GRCh38.p12 chr21: 33,322,493-33,322,992 IFNAR1
    nsv6125241insertion1nstd186human GRCh37 chrX: 1,393,469-1,393,469 , GRCh38.p12 chrX: 1,274,576-1,274,576 CSF2RA
    nsv6122201copy number variation1nstd186human GRCh37 chr10: 6,097,386-6,097,868 , GRCh38.p12 chr10: 6,055,423-6,055,905 IL2RA
    nsv6121591copy number variation1nstd186human GRCh37 chr16: 27,462,363-27,462,460 , GRCh38.p12 chr16: 27,451,042-27,451,139 IL21R, IL21R-AS1
    nsv6120911copy number variation1nstd186human GRCh37 chr13: 28,625,931-28,626,481 , GRCh38.p12 chr13: 28,051,794-28,052,344 FLT3
    nsv6120125copy number variation1nstd186human GRCh37 chr2: 203,295,143-203,312,893 , GRCh38.p12 chr2: 202,430,420-202,448,170 BMPR2
    nsv6116896copy number variation1nstd186human GRCh37 chrX: 1,433,437-1,433,744 , GRCh38.p12 chrX: 1,314,544-1,314,851 CSF2RA
    nsv6116729copy number variation1nstd186human GRCh37 chrX: 1,487,593-1,495,244 , GRCh38.p12 chrX: 1,368,700-1,376,351 , IL3RA
    nsv6116618copy number variation1nstd186human GRCh37 chrX: 1,403,325-1,403,575 , GRCh38.p12 chrX: 1,284,432-1,284,682 CSF2RA
    nsv6116355copy number variation1nstd186human GRCh37 chrX: 1,406,545-1,406,839 , GRCh38.p12 chrX: 1,287,652-1,287,946 CSF2RA
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