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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
    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
    nsv6765635copy number variation1nstd229human GRCh38 chr5: 76,299,101-77,533,100 , GRCh37.p13 chr5: 75,594,926-76,828,925 SNRPCP2, RNU6ATAC36P, 20 more genes
    nsv6637134copy number variation1nstd102humanUncertain significance GRCh37 chr5: 76,239,549-76,720,244 , GRCh38.p12 chr5: 76,943,724-77,424,419 AGGF1, CRHBP, 8 more genes
    nsv6630441copy number variation1nstd224human GRCh37 chr5: 75,820,998-76,444,754 , GRCh38.p12 chr5: 76,525,173-77,148,929 SNORA47, LOC101929109, 13 more genes
    nsv6410203copy number variation1nstd223human GRCh38 chr5: 77,022,601-77,101,400 , GRCh37.p13 chr5: 76,318,426-76,397,225 AGGF1, SNORA47, 2 more genes
    nsv6405430copy number variation1nstd223human GRCh38 chr5: 76,901,982-77,120,694 , GRCh37.p13 chr5: 76,197,807-76,416,519 RNU6ATAC36P, AGGF1, 5 more genes
    nsv6136132copy number variation1nstd213human GRCh37 chr5: 73,950,000-76,390,001 , GRCh38.p12 chr5: 74,654,175-77,094,176 CRHBP, F2R, 52 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
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    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
    nsv4591595copy number variation1nstd183human GRCh37 chr5: 76,088,861-76,547,813 , GRCh38.p12 chr5: 76,793,036-77,251,988 ZBED3-AS1, SNORA47, 9 more genes
    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
    nsv4409411copy number variation1nstd174human GRCh37 chr5: 76,190,936-76,414,733 , GRCh38.p12 chr5: 76,895,111-77,118,908 CRHBP, AGGF1, 5 more genes
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv3957917copy number variation1nstd168human GRCh38 chr5: 77,078,407-77,104,202 , GRCh37.p13 chr5: 76,374,232-76,400,027 SNORA47, ZBED3, 1 more genes
    nsv3917856copy number variation1nstd102humanPathogenic GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153 CSNK1A1P3, POLR3G, 413 more genes
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