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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933809copy number variation1nstd209human GRCh38 chr19: 42,436,057-42,436,202 , GRCh37.p13 chr19: 42,940,209-42,940,354 LIPE-AS1, CXCL17
    nsv5591056copy number variation1nstd207human GRCh38 chr19: 42,436,057-42,436,202 , GRCh37.p13 chr19: 42,940,209-42,940,354 LIPE-AS1, CXCL17
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5522493copy number variation1nstd206human GRCh38 chr19: 42,436,057-42,436,203 , GRCh37.p13 chr19: 42,940,209-42,940,355 CXCL17, LIPE-AS1
    nsv5362306translocation1nstd200human GRCh38 chr19: 42,428,303-42,428,303 , GRCh38 chr5: 66,179,495-66,179,495 , GRCh37.p13 chr19: 42,932,455-42,932,455 , GRCh37.p13 chr5: 65,475,323-65,475,323 SREK1, CXCL17, 1 more genes
    nsv5362305translocation1nstd200human GRCh38 chr19: 42,428,305-42,428,305 , GRCh38 chr5: 66,178,881-66,178,881 , GRCh37.p13 chr19: 42,932,457-42,932,457 , GRCh37.p13 chr5: 65,474,709-65,474,709 SREK1, CXCL17, 1 more genes
    nsv5323339copy number variation1nstd204human GRCh37.p13 chr19: 42,940,204-42,940,359 , GRCh38.p13 chr19: 42,436,052-42,436,207 CXCL17, LIPE-AS1
    nsv5165556mobile element insertion1nstd203human GRCh38 chr19: 42,438,354-42,438,382 , GRCh37.p13 chr19: 42,942,506-42,942,534 CXCL17, LIPE-AS1
    nsv5020532copy number variation1nstd200human GRCh38 chr19: 42,424,141-42,427,054 , GRCh37.p13 chr19: 42,928,293-42,931,206 LIPE-AS1, CXCL17, 1 more genes
    nsv4868458copy number variation1nstd200human GRCh37 chr19: 42,928,293-42,931,206 , GRCh38.p12 chr19: 42,424,141-42,427,054 LIPE, CXCL17, 1 more genes
    nsv4715396copy number variation1nstd195human GRCh38.p12 chr19: 42,419,999-42,609,899 , GRCh37 chr19: 42,924,151-43,114,051 CEACAM1, CEACAM8, 7 more genes
    nsv4637793copy number variation2nstd186human GRCh37 chr19: 42,940,209-42,940,355 , GRCh38.p12 chr19: 42,436,057-42,436,203 CXCL17, LIPE-AS1
    nsv4535646copy number variation1nstd166human GRCh37.p13 chr19: 42,940,209-42,940,355 , GRCh38.p12 chr19: 42,436,057-42,436,203 CXCL17, LIPE-AS1
    nsv4534722copy number variation1nstd166human GRCh37.p13 chr19: 42,930,999-43,263,000 , GRCh38.p12 chr19: 42,426,847-42,758,848 LIPE, CXCL17, 12 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4271299copy number variation1nstd166human GRCh37.p13 chr19: 42,941,647-42,942,146 , GRCh38.p12 chr19: 42,437,495-42,437,994 CXCL17, LIPE-AS1
    nsv4266017copy number variation1nstd166human GRCh37.p13 chr19: 42,931,000-42,962,000 , GRCh38.p12 chr19: 42,426,848-42,457,848 LIPE-AS1, LIPE, 1 more genes
    nsv4259973copy number variation1nstd166human GRCh37.p13 chr19: 42,937,017-43,829,931 , GRCh38.p12 chr19: 42,432,865-43,325,779 , CEACAM8, 31 more genes
    nsv3921916copy number variation1nstd102humanPathogenic NCBI36 chr19: 47,126,886-48,337,448 , GRCh37 chr19: 42,514,712-43,645,608 , GRCh38 chr19: 41,930,894-43,141,456 PSG6, RABAC1, 42 more genes
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