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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040988inversion1nstd229human GRCh38 chr2: 211,965-587,054 , GRCh37.p13 chr2: 211,965-587,054 LOC100996637, ACP1, 9 more genes
    nsv6677781copy number variation1nstd229human GRCh38 chr2: 286,038-295,058 , GRCh37.p13 chr2: 286,038-295,058 LOC101927262, ALKAL2, 1 more genes
    nsv6676374copy number variation1nstd229human GRCh38 chr2: 83,465-311,366 , GRCh37.p13 chr2: 83,465-311,366 SH3YL1, ALKAL2, 4 more genes
    nsv6676031copy number variation1nstd229human GRCh38 chr2: 71,486-302,675 , GRCh37.p13 chr2: 71,486-302,675 ACP1, LOC105373324, 4 more genes
    nsv6673666copy number variation1nstd229human GRCh38 chr2: 123,856-436,360 , GRCh37.p13 chr2: 123,856-436,360 LOC105373346, ACP1, 6 more genes
    nsv6672477copy number variation1nstd229human GRCh38 chr2: 197,164-655,134 , GRCh37.p13 chr2: 197,164-655,134 LOC100996637, ACP1, 9 more genes
    nsv6672028copy number variation1nstd229human GRCh38 chr2: 281,298-525,445 , GRCh37.p13 chr2: 281,298-525,445 LOC105373351, LINC01874, 5 more genes
    nsv6668500copy number variation1nstd229human GRCh38 chr2: 200,795-393,526 , GRCh37.p13 chr2: 200,795-393,526 LOC105373351, ACP1, 5 more genes
    nsv6667961copy number variation1nstd229human GRCh38 chr2: 287,832-619,733 , GRCh37.p13 chr2: 287,832-619,733 LOC100996637, LOC105373352, 7 more genes
    nsv6665613copy number variation1nstd229human GRCh38 chr2: 282,654-282,963 , GRCh37.p13 chr2: 282,654-282,963 ALKAL2
    nsv6660023copy number variation1nstd229human GRCh38 chr2: 119,838-339,507 , GRCh37.p13 chr2: 119,838-339,507 LOC101927262, ALKAL2, 5 more genes
    nsv6659090copy number variation1nstd229human GRCh38 chr2: 268,580-763,147 , GRCh37.p13 chr2: 268,580-763,147 ALKAL2, LINC01875, 13 more genes
    nsv6636363copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,771-1,947,832 , GRCh38.p12 chr2: 12,771-1,944,060 LOC105373352, LOC105373346, 26 more genes
    nsv6555528inversion1nstd223human GRCh38 chr2: 60,564-381,949 , GRCh37.p13 chr2: 60,564-381,949 ACP1, SH3YL1, 6 more genes
    nsv6325759copy number variation1nstd223human GRCh38 chr2: 197,016-655,135 , GRCh37.p13 chr2: 197,016-655,135 LOC105373351, LINC01875, 9 more genes
    nsv6321692copy number variation1nstd223human GRCh38 chr2: 264,180-313,687 , GRCh37.p13 chr2: 264,180-313,687 ALKAL2, LOC101927262, 3 more genes
    nsv6321644copy number variation1nstd223human GRCh38 chr2: 214,401-293,900 , GRCh37.p13 chr2: 214,401-293,900 ALKAL2, SH3YL1, 3 more genes
    nsv6317336copy number variation1nstd223human GRCh38 chr2: 268,580-763,147 , GRCh37.p13 chr2: 268,580-763,147 LOC105373352, LOC105373346, 13 more genes
    nsv6316255copy number variation1nstd223human GRCh38 chr2: 27,263-377,948 , GRCh37.p13 chr2: 27,263-377,948 FAM110C, LOC101927262, 7 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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