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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096788copy number variation1nstd102humanPathogenic GRCh37 chr5: 76,115,008-78,281,071 , GRCh38.p12 chr5: 76,819,183-78,985,248 LHFPL2, OTP, 27 more genes
    nsv7057779inversion1nstd229human GRCh38 chr5: 77,504,364-78,172,473 , GRCh37.p13 chr5: 76,800,189-77,468,297 OTP, TBCA, 8 more genes
    nsv7050643inversion1nstd229human GRCh38 chr5: 77,339,476-78,646,078 , GRCh37.p13 chr5: 76,635,301-77,941,901 LHFPL2, RNU6-183P, 15 more genes
    nsv7045119inversion1nstd229human GRCh38 chr5: 76,735,197-79,503,040 , GRCh37.p13 chr5: 76,031,022-78,798,863 RNU6ATAC36P, RPS3AP20, 39 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv7040636inversion1nstd229human GRCh38 chr5: 76,863,641-77,977,772 , GRCh37.p13 chr5: 76,159,466-77,273,596 LOC101929154, ZBED3, 15 more genes
    nsv7038776inversion1nstd229human GRCh38 chr5: 76,735,364-79,502,930 , GRCh37.p13 chr5: 76,031,189-78,798,753 HOMER1, LOC100505796, 39 more genes
    nsv6766373copy number variation1nstd229human GRCh38 chr5: 77,639,177-77,642,866 , GRCh37.p13 chr5: 76,935,002-76,938,691 OTP
    nsv6411736copy number variation1nstd223human GRCh38 chr5: 77,619,801-77,660,600 , GRCh37.p13 chr5: 76,915,626-76,956,425 WDR41, OTP
    nsv6408582copy number variation1nstd223human GRCh38 chr5: 77,596,501-77,883,300 , GRCh37.p13 chr5: 76,892,326-77,179,124 LOC101929154, OTP, 3 more genes
    nsv6400602copy number variation1nstd223human GRCh38 chr5: 77,626,801-77,629,500 , GRCh37.p13 chr5: 76,922,626-76,925,325 OTP
    nsv6135682copy number variation1nstd213human GRCh37 chr5: 76,540,000-78,280,001 , GRCh38.p12 chr5: 77,244,175-78,984,178 ACTBP2, ARSB, 17 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv5087679mobile element insertion1nstd203human GRCh38 chr5: 77,634,519-77,634,531 , GRCh37.p13 chr5: 76,930,344-76,930,356 OTP
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4937902copy number variation1nstd200human GRCh38 chr5: 77,636,548-77,636,705 , GRCh37.p13 chr5: 76,932,373-76,932,530 OTP
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4556239insertion1nstd166human GRCh37.p13 chr5: 76,930,344-76,930,344 , GRCh38.p12 chr5: 77,634,519-77,634,519 OTP
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
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