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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5555882sequence alteration1nstd206human GRCh38 chr19: 45,580,124-46,272,839 , GRCh37.p13 chr19: 46,083,382-46,776,096 , SYMPK, 39 more genes
    nsv5517421copy number variation1nstd206human GRCh38 chr19: 45,673,184-45,675,614 , GRCh37.p13 chr19: 46,176,442-46,178,872 MIR642B, MIR642A, 1 more genes
    nsv5327341copy number variation1nstd204human GRCh38.p13 chr19: 45,584,936-45,884,300 , GRCh37.p13 chr19: 46,088,194-46,387,558 DMWD, GPR4, 19 more genes
    nsv5291484copy number variation1nstd204human GRCh38.p13 chr19: 45,671,142-45,678,919 , GRCh37.p13 chr19: 46,174,400-46,182,177 MIR642A, GIPR, 1 more genes
    nsv5284788copy number variation1nstd204human GRCh38.p13 chr19: 45,504,601-45,776,400 , GRCh37.p13 chr19: 46,007,859-46,279,658 MIR642A, LOC107985315, 17 more genes
    nsv5024731copy number variation1nstd200human GRCh38 chr19: 45,652,324-45,724,747 , GRCh37.p13 chr19: 46,155,582-46,228,005 QPCTL, MIR642A, 4 more genes
    nsv5020706copy number variation1nstd200human GRCh38 chr19: 45,673,419-45,673,531 , GRCh37.p13 chr19: 46,176,677-46,176,789 MIR642B, GIPR, 1 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 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
    nsv4260638copy number variation1nstd166human GRCh37.p13 chr19: 46,164,182-46,177,331 , GRCh38.p12 chr19: 45,660,924-45,674,073 GIPR, MIR642B, 1 more genes
    nsv4256969copy number variation1nstd166human GRCh37.p13 chr19: 46,178,712-46,179,011 , GRCh38.p12 chr19: 45,675,454-45,675,753 GIPR, MIR642A, 1 more genes
    nsv3924836copy number variation1nstd102humanPathogenic NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402 IGFL1P1, LOC105372426, 145 more genes
    nsv3924271copy number variation1nstd102humanUncertain significance GRCh38 chr19: 45,481,858-45,710,518 , GRCh37 chr19: 45,985,116-46,213,776 , NCBI36 chr19: 50,676,956-50,905,616 RN7SL836P, MIR642B, 15 more genes
    nsv3921787copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 50,582,487-52,026,097 , GRCh37 chr19: 45,890,647-47,334,257 , GRCh38 chr19: 45,387,389-46,831,000 CALM3, DMPK, 71 more genes
    nsv3921263copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,790,514-46,237,336 , NCBI36 chr19: 50,482,354-50,929,176 , GRCh38 chr19: 45,287,256-45,734,078 MIR642A, ERCC2, 26 more genes
    nsv3916206copy number variation1nstd102humanPathogenic GRCh37 chr19: 46,099,131-47,103,283 , NCBI36 chr19: 50,790,971-51,795,123 , GRCh38 chr19: 45,595,873-46,600,026 PNMA8B, MIR642B, 47 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
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