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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095645copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315 HAUS8, MIR1470, 95 more genes
    nsv7075473inversion1nstd229human GRCh38 chr19: 12,694,752-17,614,167 , GRCh37.p13 chr19: 12,805,566-17,724,976 SYDE1, LOC107985287, 207 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7063135inversion1nstd229human GRCh38 chr19: 12,625,698-17,530,884 , GRCh37.p13 chr19: 12,736,512-17,641,693 SYCE2, OR1AB1P, 212 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7009063copy number variation1nstd229human GRCh38 chr19: 17,207,614-17,239,395 , GRCh37.p13 chr19: 17,318,423-17,350,204 USE1, MYO9B, 2 more genes
    nsv7005523copy number variation1nstd229human GRCh38 chr19: 17,218,305-17,232,786 , GRCh37.p13 chr19: 17,329,114-17,343,595 USE1, OCEL1, 1 more genes
    nsv7004911copy number variation1nstd229human GRCh38 chr19: 16,817,573-17,564,195 , GRCh37.p13 chr19: 16,928,384-17,675,004 BISPR, NWD1, 32 more genes
    nsv6624836copy number variation1nstd224human GRCh37 chr19: 17,321,596-17,339,699 , GRCh38.p12 chr19: 17,210,787-17,228,890 MYO9B, OCEL1, 1 more genes
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6529933copy number variation1nstd223human GRCh38 chr19: 17,207,855-17,216,777 , GRCh37.p13 chr19: 17,318,664-17,327,586 MYO9B, USE1
    nsv6524172copy number variation1nstd223human GRCh38 chr19: 17,216,758-17,222,603 , GRCh37.p13 chr19: 17,327,567-17,333,412 USE1
    nsv6133691copy number variation1nstd213human GRCh37 chr19: 15,360,000-18,450,001 , GRCh38.p12 chr19: 15,249,189-18,339,191 BST2, NR2F6, 123 more genes
    nsv6133521copy number variation1nstd213human GRCh37 chr19: 17,200,000-17,780,001 , GRCh38.p12 chr19: 17,089,190-17,669,192 ANO8, OCEL1, 27 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5299651copy number variation1nstd204human GRCh38.p13 chr19: 16,996,101-18,292,600 , GRCh37.p13 chr19: 17,106,911-18,403,410 ANO8, MPV17L2, 57 more genes
    nsv5293042copy number variation1nstd204human GRCh38.p13 chr19: 17,178,501-17,350,400 , GRCh37.p13 chr19: 17,289,310-17,461,209 NR2F6, ABHD8, 11 more genes
    nsv5286520copy number variation1nstd204human GRCh38.p13 chr19: 17,091,201-17,638,100 , GRCh37.p13 chr19: 17,202,011-17,748,909 PGLS, LOC105372298, 27 more genes
    nsv5164925mobile element insertion1nstd203human GRCh38 chr19: 17,216,760-17,216,776 , GRCh37.p13 chr19: 17,327,569-17,327,585 USE1
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