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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7073355inversion1nstd229human GRCh38 chr19: 38,760,450-38,833,692 , GRCh37.p13 chr19: 39,251,090-39,324,332 LGALS7B, RNU6-140P, 3 more genes
    nsv7072429inversion1nstd229human GRCh38 chr19: 38,777,411-38,800,222 , GRCh37.p13 chr19: 39,268,051-39,290,862 LGALS4, LGALS7B, 1 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002068copy number variation1nstd229human GRCh38 chr19: 38,758,871-38,818,740 , GRCh37.p13 chr19: 39,249,511-39,309,380 RNU6-140P, ECH1, 3 more genes
    nsv7001253copy number variation1nstd229human GRCh38 chr19: 38,813,072-38,813,250 , GRCh37.p13 chr19: 39,303,712-39,303,890 LGALS4
    nsv6598254inversion1nstd223human GRCh38 chr19: 38,808,676-38,809,141 , GRCh37.p13 chr19: 39,299,316-39,299,781 LGALS4
    nsv6526448copy number variation1nstd223human GRCh38 chr19: 38,758,834-38,818,779 , GRCh37.p13 chr19: 39,249,474-39,309,419 LGALS4, LGALS7, 3 more genes
    nsv6518144copy number variation1nstd223human GRCh38 chr19: 38,809,249-38,810,432 , GRCh37.p13 chr19: 39,299,889-39,301,072 LGALS4
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6101177insertion1nstd212human GRCh38 chr19: 38,810,642-38,810,642 , GRCh37.p13 chr19: 39,301,282-39,301,282 LGALS4
    nsv6054206copy number variation1nstd212human GRCh38 chr19: 38,808,461-38,808,547 , GRCh37.p13 chr19: 39,299,101-39,299,187 LGALS4
    nsv6041873copy number variation1nstd212human GRCh38 chr19: 38,809,252-38,809,363 , GRCh37.p13 chr19: 39,299,892-39,300,003 LGALS4
    nsv5027897copy number variation1nstd200human GRCh38 chr19: 38,809,269-38,810,442 , GRCh37.p13 chr19: 39,299,909-39,301,082 LGALS4
    nsv5024622copy number variation1nstd200human GRCh38 chr19: 38,758,799-38,818,817 , GRCh37.p13 chr19: 39,249,439-39,309,457 LGALS7, LGALS4, 3 more genes
    nsv4865159copy number variation1nstd200human GRCh37 chr19: 39,249,439-39,309,457 , GRCh38.p12 chr19|NW_014040929.1: 168,408-228,489 , GRCh38.p12 chr19: 38,758,799-38,818,817 ECH1, RNU6-140P, 3 more genes
    nsv4746866copy number variation1nstd199human GRCh37 chr19: 39,299,084-39,299,187 , GRCh38.p12 chr19|NW_014040929.1: 218,116-218,219 , GRCh38.p12 chr19: 38,808,444-38,808,547 LGALS4
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