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Items: 1 to 20 of 336

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7045006inversion1nstd229human GRCh38 chr2: 28,892,565-29,348,187 , GRCh37.p13 chr2: 29,115,431-29,571,053 SNORD92, LOC105374386, 8 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv7042078inversion1nstd229human GRCh38 chr2: 29,181,383-29,181,871 , GRCh37.p13 chr2: 29,404,249-29,404,737 CLIP4
    nsv6676432copy number variation1nstd229human GRCh38 chr2: 29,099,670-29,106,097 , GRCh37.p13 chr2: 29,322,536-29,328,963 CLIP4
    nsv6673802copy number variation1nstd229human GRCh38 chr2: 29,128,435-29,132,340 , GRCh37.p13 chr2: 29,351,301-29,355,206 CLIP4
    nsv6672959copy number variation1nstd229human GRCh38 chr2: 29,098,868-29,105,752 , GRCh37.p13 chr2: 29,321,734-29,328,618 CLIP4
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6666251copy number variation1nstd229human GRCh38 chr2: 29,140,027-29,184,038 , GRCh37.p13 chr2: 29,362,893-29,406,904 CLIP4
    nsv6665753copy number variation1nstd229human GRCh38 chr2: 29,152,460-29,154,917 , GRCh37.p13 chr2: 29,375,326-29,377,783 CLIP4
    nsv6660145copy number variation1nstd229human GRCh38 chr2: 29,107,601-29,111,800 , GRCh37.p13 chr2: 29,330,467-29,334,666 CLIP4
    nsv6658568copy number variation1nstd229human GRCh38 chr2: 28,879,126-29,482,143 , GRCh37.p13 chr2: 29,101,992-29,705,009 LOC101929386, SNORD92, 9 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 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
    nsv6628048copy number variation1nstd224human GRCh37 chr2: 29,312,240-29,366,627 , GRCh38.p12 chr2: 29,089,374-29,143,761 CLIP4, LOC105374386
    nsv6546927inversion1nstd223human GRCh38 chr2: 26,476,473-32,916,584 , GRCh37.p13 chr2: 26,699,341-33,141,651 LOC105374453, LCLAT1, 129 more genes
    nsv6546310inversion1nstd223human GRCh38 chr2: 29,139,769-29,140,072 , GRCh37.p13 chr2: 29,362,635-29,362,938 CLIP4
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538559inversion1nstd223human GRCh38 chr2: 25,762,333-32,867,002 , GRCh37.p13 chr2: 25,985,202-33,092,069 MIR558, PCARE, 148 more genes
    nsv6352804copy number variation1nstd223human GRCh38 chr2: 29,143,412-29,144,798 , GRCh37.p13 chr2: 29,366,278-29,367,664 CLIP4
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