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Items: 1 to 20 of 417

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5974394inversion1nstd209human GRCh38 chr4: 4,005,086-9,639,734 , GRCh37.p13 chr4: 4,006,813-9,641,358 , CRMP1, 142 more genes
    nsv5906200copy number variation1nstd209human GRCh38 chr4: 9,159,413-9,696,820 , GRCh37.p13 chr4: 9,161,139-9,698,444 USP17L27, FAM90A26, 41 more genes
    nsv5895914copy number variation1nstd209human GRCh38 chr4: 9,143,882-9,680,194 , GRCh37.p13 chr4: 9,145,608-9,681,818 USP17L14P, USP17L5, 41 more genes
    nsv5840221copy number variation1nstd209human GRCh38 chr4: 9,513,110-9,518,642 , GRCh37.p13 chr4: 9,514,759-9,520,287 OR7E83P
    nsv5617518insertion1nstd207human GRCh38 chr4: 9,511,599-9,511,599 , GRCh37.p13 chr4: 9,513,248-9,513,248 OR7E83P
    nsv5615132insertion1nstd207human GRCh38 chr4: 9,510,916-9,510,916 , GRCh37.p13 chr4: 9,512,565-9,512,565 OR7E83P
    nsv5444642copy number variation1nstd206human GRCh38 chr4: 9,322,916-9,809,500 , GRCh37.p13 chr4: 9,324,643-9,811,124 SLC2A9, OR7E86P, 31 more genes
    nsv5443611copy number variation1nstd206human GRCh38 chr4: 9,485,353-9,514,517 , GRCh37.p13 chr4: 9,487,000-9,516,166 OR7E83P, UNC93B7
    nsv5315674copy number variation1nstd204human GRCh38.p13 chr4: 9,158,575-9,697,142 , GRCh37.p13 chr4: 9,160,301-9,698,766 RNA5SP153, USP17L15, 41 more genes
    nsv5312228copy number variation1nstd204human GRCh38.p13 chr4: 9,157,539-9,696,164 , GRCh37.p13 chr4: 9,159,265-9,697,788 USP17L6P, ENPP7P11, 41 more genes
    nsv5235289copy number variation1nstd204human GRCh38.p13 chr4: 9,500,870-9,515,372 , GRCh37.p13 chr4: 9,502,514-9,517,014 OR7E83P
    nsv5225173copy number variation1nstd204human GRCh38.p13 chr4: 9,489,577-9,515,882 , GRCh37.p13 chr4: 9,491,221-9,517,524 OR7E83P, UNC93B7
    nsv4925260copy number variation1nstd200human GRCh38 chr4: 9,489,973-9,519,453 , GRCh37.p13 chr4: 9,491,617-9,521,098 UNC93B7, OR7E83P
    nsv4925258copy number variation1nstd200human GRCh38 chr4: 9,449,564-9,696,422 , GRCh37.p13 chr4: 9,451,290-9,698,046 OR7E86P, SNRPCP13, 11 more genes
    nsv4925254copy number variation1nstd200human GRCh38 chr4: 9,114,621-9,651,161 , GRCh37.p13 chr4: 9,116,347-9,652,785 USP17L12, DEFB131A, 41 more genes
    nsv4925252copy number variation1nstd200human GRCh38 chr4: 9,054,261-9,586,566 , GRCh37.p13 chr4: 9,055,987-9,588,190 OR7E85P, USP17L27, 41 more genes
    nsv4925247copy number variation1nstd200human GRCh38 chr4: 8,880,941-9,829,738 , GRCh37.p13 chr4: 8,882,667-9,831,362 FAM86MP, FAM90A26, 54 more genes
    nsv4925243copy number variation1nstd200human GRCh38 chr4: 8,427,161-10,250,688 , GRCh37.p13 chr4: 8,428,888-10,252,312 , OR7E35P, 68 more genes
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