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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7016235copy number variation1nstd229human GRCh38 chr19: 9,307,301-9,310,100 , GRCh37.p13 chr19: 9,417,977-9,420,776 ZNF699
    nsv7015671copy number variation1nstd229human GRCh38 chr19: 9,290,735-9,304,682 , GRCh37.p13 chr19: 9,401,411-9,415,358 ZNF699
    nsv7012246copy number variation1nstd229human GRCh38 chr19: 9,202,317-9,299,718 , GRCh37.p13 chr19: 9,312,993-9,410,394 OR7E24, OR7D4, 7 more genes
    nsv7011275copy number variation1nstd229human GRCh38 chr19: 9,304,841-9,315,319 , GRCh37.p13 chr19: 9,415,517-9,425,995 ZNF699
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv6596272inversion1nstd223human GRCh38 chr19: 9,291,729-9,293,036 , GRCh37.p13 chr19: 9,402,405-9,403,712 ZNF699
    nsv6523763copy number variation1nstd223human GRCh38 chr19: 9,304,841-9,315,319 , GRCh37.p13 chr19: 9,415,517-9,425,995 ZNF699
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5980087insertion1nstd209human GRCh38 chr19: 9,305,265-9,305,265 , GRCh37.p13 chr19: 9,415,941-9,415,941 ZNF699
    nsv5944384copy number variation1nstd209human GRCh38 chr19: 9,298,145-9,298,452 , GRCh37.p13 chr19: 9,408,821-9,409,128 ZNF699
    nsv5929829copy number variation1nstd209human GRCh38 chr19: 9,304,841-9,315,318 , GRCh37.p13 chr19: 9,415,517-9,425,994 ZNF699
    nsv5523041copy number variation1nstd206human GRCh38 chr19: 9,304,841-9,315,320 , GRCh37.p13 chr19: 9,415,517-9,425,996 ZNF699
    nsv5328693copy number variation1nstd204human GRCh38.p13 chr19: 9,296,383-9,296,716 , GRCh37.p13 chr19: 9,407,059-9,407,392 ZNF699
    nsv5206766mobile element deletion1nstd204human GRCh38.p13 chr19: 9,298,138-9,298,481 , GRCh37.p13 chr19: 9,408,814-9,409,157 ZNF699
    nsv4907492mobile element deletion1nstd200human GRCh38 chr19: 9,298,167-9,298,453 , GRCh37.p13 chr19: 9,408,843-9,409,129 ZNF699
    nsv4864910copy number variation1nstd200human GRCh37 chr19: 9,415,516-9,425,997 , GRCh38.p12 chr19: 9,304,840-9,315,321 ZNF699
    nsv4769738mobile element deletion1nstd200human GRCh37 chr19: 9,408,843-9,409,129 , GRCh38.p12 chr19: 9,298,167-9,298,453 ZNF699
    nsv4729955copy number variation1nstd102humanLikely benign GRCh37 chr19: 9,245,167-9,465,565 , GRCh38.p12 chr19: 9,134,491-9,354,889 ZNF699, ZNF559-ZNF177, 14 more genes
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
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