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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053537inversion1nstd229human GRCh38 chr2: 96,159,639-96,243,155 , GRCh37.p13 chr2: 96,825,377-96,908,893 STARD7, SNORA112, 1 more genes
    nsv6694106copy number variation1nstd229human GRCh38 chr2: 96,211,438-96,225,422 , GRCh37.p13 chr2: 96,877,176-96,891,160 SNORA112, STARD7-AS1
    nsv6689215copy number variation1nstd229human GRCh38 chr2: 96,207,600-96,207,887 , GRCh37.p13 chr2: 96,873,338-96,873,625 STARD7-AS1, STARD7
    nsv6685563copy number variation1nstd229human GRCh38 chr2: 96,226,256-96,233,777 , GRCh37.p13 chr2: 96,891,994-96,899,515 STARD7-AS1
    nsv6637051copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,628,608-96,981,369 , GRCh38.p12 chr2: 95,962,860-96,315,631 FAHD2CP, ASTL, 12 more genes
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628429copy number variation1nstd224human GRCh37 chr2: 96,747,466-98,186,298 , GRCh38.p12 chr2: 96,081,718-97,569,835 ARID5A, IGKV2OR2-2, 42 more genes
    nsv6628179copy number variation1nstd224human GRCh37 chr2: 96,721,808-98,186,298 , GRCh38.p12 chr2: 96,056,060-97,569,835 ADRA2B, IGKV2OR2-10, 43 more genes
    nsv6554446inversion1nstd223human GRCh38 chr2: 96,223,576-96,224,559 , GRCh37.p13 chr2: 96,889,314-96,890,297 STARD7-AS1
    nsv6552359inversion1nstd223human GRCh38 chr2: 96,210,255-96,219,724 , GRCh37.p13 chr2: 96,875,993-96,885,462 STARD7-AS1, SNORA112
    nsv6547092inversion1nstd223human GRCh38 chr2: 96,007,660-97,097,743 , GRCh37.p13 chr2: 96,673,408-97,763,480 CNNM4, DUSP2, 34 more genes
    nsv6541958inversion1nstd223human GRCh38 chr2: 96,215,191-96,215,626 , GRCh37.p13 chr2: 96,880,929-96,881,364 SNORA112, STARD7-AS1
    nsv6349234copy number variation1nstd223human GRCh38 chr2: 96,226,251-96,233,776 , GRCh37.p13 chr2: 96,891,989-96,899,514 STARD7-AS1
    nsv6349233copy number variation1nstd223human GRCh38 chr2: 96,210,301-96,215,500 , GRCh37.p13 chr2: 96,876,039-96,881,238 STARD7-AS1, SNORA112
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6311431copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,780,545-97,475,254 , GRCh38.p12 chr2: 96,114,797-96,809,517 LOC105373496, STARD7-AS1, 17 more genes
    nsv6290784copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,544,603-98,025,634 , GRCh38.p12 chr2: 95,878,855-97,285,797 LOC100506076, FAHD2B, 39 more genes
    nsv6134374copy number variation1nstd213human GRCh37 chr2: 95,650,000-97,860,001 , GRCh38.p12 chr2: 94,984,255-97,194,264 ADRA2B, DUSP2, 68 more genes
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