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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077968inversion1nstd229human GRCh38 chr19: 14,024,678-14,298,986 , GRCh37.p13 chr19: 14,135,490-14,409,798 PRKACA, SAMD1, 11 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
    nsv7058723inversion1nstd229human GRCh38 chr19: 13,672,973-14,832,292 , GRCh37.p13 chr19: 13,783,787-14,943,104 SNRPGP15, NDUFB7, 53 more genes
    nsv7009275copy number variation1nstd229human GRCh38 chr19: 13,836,899-14,088,244 , GRCh37.p13 chr19: 13,947,713-14,199,056 NANOS3, RLN3, 17 more genes
    nsv7004641copy number variation1nstd229human GRCh38 chr19: 14,016,810-14,348,943 , GRCh37.p13 chr19: 14,127,622-14,459,755 PRKACA, LINC01841, 13 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
    nsv6133690copy number variation1nstd213human GRCh37 chr19: 13,260,000-16,840,001 , GRCh38.p12 chr19: 13,149,186-16,729,190 PRKACA, SLC1A6, 137 more genes
    nsv6133467copy number variation1nstd213human GRCh37 chr19: 14,110,000-14,470,001 , GRCh38.p12 chr19: 13,999,188-14,359,189 SAMD1, EEF1DP1, 14 more genes
    nsv6048648copy number variation1nstd212human GRCh38 chr19: 14,068,040-14,068,346 , GRCh37.p13 chr19: 14,178,852-14,179,158 EEF1DP1
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5300223copy number variation1nstd204human GRCh38.p13 chr19: 13,638,301-14,767,500 , GRCh37.p13 chr19: 13,749,115-14,878,312 , SNORA104, 53 more genes
    nsv5295552copy number variation1nstd204human GRCh38.p13 chr19: 13,937,101-14,461,200 , GRCh37.p13 chr19: 14,047,914-14,572,012 , ASF1B, 20 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4425330copy number variation1nstd174human GRCh37 chr19: 14,170,554-14,321,100 , GRCh38.p12 chr19: 14,059,742-14,210,288 ADGRL1, ASF1B, 8 more genes
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
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