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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4947135copy number variation1nstd200human GRCh38 chr5: 90,409,144-90,413,140 , GRCh37.p13 chr5: 89,704,961-89,708,957 LOC731157, CETN3
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4681100copy number variation1nstd102humanUncertain significance GRCh37 chr5: 89,689,881-90,107,155 , GRCh38.p12 chr5: 90,394,064-90,811,338 LOC105379077, ADGRV1, 5 more genes
    nsv4675924copy number variation1nstd102humanUncertain significance GRCh37 chr5: 87,611,415-89,975,436 , GRCh38.p12 chr5: 88,315,598-90,679,619 RPS3AP22, LYSMD3, 20 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
    nsv4675472copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143 CAST, CETN3, 202 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
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 more genes
    nsv3924896copy number variation1nstd102humanPathogenic GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678 LOC107986438, GGCTP1, 254 more genes
    nsv3922083copy number variation1nstd102humanPathogenic GRCh38 chr5: 86,766,959-92,148,845 , GRCh37 chr5: 86,062,776-91,444,662 , NCBI36 chr5: 86,098,532-91,480,418 LOC107986387, RN7SL629P, 52 more genes
    nsv3921368copy number variation1nstd102humanPathogenic GRCh37 chr5: 86,672,700-100,860,147 , NCBI36 chr5: 86,708,456-100,888,046 , GRCh38 chr5: 87,376,883-101,524,443 LOC107986438, MTCO1P22, 158 more genes
    nsv3921192copy number variation1nstd102humanPathogenic NCBI36 chr5: 89,559,719-90,448,165 , GRCh37 chr5: 89,523,963-90,412,409 , GRCh38 chr5: 90,228,146-91,116,592 CETN3, POLR3G, 7 more genes
    nsv3919032copy number variation1nstd102humanUncertain significance NCBI36 chr5: 89,443,896-89,982,204 , GRCh37.p13 chr5: 89,408,140-89,946,448 , GRCh38.p12 chr5: 90,112,323-90,650,631 LOC731157, ADGRV1, 5 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
    nsv3917287copy number variation1nstd102humanPathogenic GRCh37 chr5: 86,420,655-92,718,726 , NCBI36 chr5: 86,456,411-92,744,482 , GRCh38 chr5: 87,124,838-93,383,020 LOC731157, LOC105379066, 55 more genes
    nsv3916982copy number variation1nstd102humanLikely benign NCBI36 chr5: 89,489,275-89,802,808 , GRCh37 chr5: 89,453,519-89,767,052 , GRCh38 chr5: 90,157,702-90,471,235 CETN3, LOC731157, 2 more genes
    nsv3916966copy number variation1nstd102humanPathogenic GRCh37 chr5: 87,664,106-91,698,938 , NCBI36 chr5: 87,699,862-91,724,694 , GRCh38 chr5: 88,368,289-92,363,231 LOC107986433, ARRDC3, 34 more genes
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