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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7013757copy number variation1nstd229human GRCh38 chr19: 33,551,601-33,554,800 , GRCh37.p13 chr19: 34,042,507-34,045,706 LOC100996681
    nsv7009871copy number variation1nstd229human GRCh38 chr19: 33,372,901-33,872,800 , GRCh37.p13 chr19: 33,863,807-34,363,705 LOC100996681, CEBPG, 5 more genes
    nsv7008006copy number variation1nstd229human GRCh38 chr19: 33,550,236-33,552,990 , GRCh37.p13 chr19: 34,041,142-34,043,896 LOC100996681
    nsv7006617copy number variation1nstd229human GRCh38 chr19: 33,527,977-33,567,464 , GRCh37.p13 chr19: 34,018,883-34,058,370 LOC100996681
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6522849copy number variation1nstd223human GRCh38 chr19: 33,547,356-33,557,823 , GRCh37.p13 chr19: 34,038,262-34,048,729 LOC100996681
    nsv6517601copy number variation1nstd223human GRCh38 chr19: 33,550,236-33,552,989 , GRCh37.p13 chr19: 34,041,142-34,043,895 LOC100996681
    nsv6517583copy number variation1nstd223human GRCh38 chr19: 33,527,977-33,567,459 , GRCh37.p13 chr19: 34,018,883-34,058,365 LOC100996681
    nsv6314074copy number variation1nstd102humanUncertain significance GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735 LOC100130632, CEP89, 59 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6209744copy number variation1nstd214human GRCh38 chr19: 33,554,461-33,554,517 , GRCh37.p13 chr19: 34,045,367-34,045,423 LOC100996681
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5929411copy number variation1nstd209human GRCh38 chr19: 33,554,461-33,554,517 , GRCh37.p13 chr19: 34,045,367-34,045,423 LOC100996681
    nsv5586652copy number variation1nstd207human GRCh38 chr19: 33,554,461-33,554,517 , GRCh37.p13 chr19: 34,045,367-34,045,423 LOC100996681
    nsv5525174copy number variation1nstd206human GRCh38 chr19: 33,425,684-34,028,349 , GRCh37.p13 chr19: 33,916,590-34,519,254 RPS4XP23, RN7SL150P, 8 more genes
    nsv5328532copy number variation1nstd204human GRCh38.p13 chr19: 33,527,974-33,567,461 , GRCh37.p13 chr19: 34,018,880-34,058,367 LOC100996681
    nsv5299999copy number variation1nstd204human GRCh38.p13 chr19: 33,528,001-33,567,400 , GRCh37.p13 chr19: 34,018,907-34,058,306 LOC100996681
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