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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148242copy number variation1nstd102humanPathogenic GRCh38 chr15: 20,966,971-25,963,714 , GRCh37.p13 chr15: 21,172,300-26,208,861 LOC101269108, LOC107983983, 227 more genes
    nsv7137131copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,833,525-23,412,276 , GRCh38.p12 chr15: 22,460,820-23,039,543 PDCD6IPP1, LOC100419579, 17 more genes
    nsv7137107copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,499-23,577,516 , GRCh38.p12 chr15: 22,358,243-23,039,569 TUBGCP5, GOLGA8IP, 22 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv6637629copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 22,770,422-23,620,154 , GRCh38.p12 chr15: 22,358,243-23,102,646 CYFIP1, NIPA2, 23 more genes
    nsv6635212copy number variation1nstd227human GRCh37 chr15: 23,272,733-23,668,092 , GRCh38.p12 chr15: 22,358,243-22,600,363 GOLGA8EP, HERC2P2, 8 more genes
    nsv6634821copy number variation1nstd227human GRCh37 chr15: 22,750,305-23,683,783 , GRCh38.p12 chr15: 22,358,243-23,122,763 CYFIP1, NIPA2, 24 more genes
    nsv6634464copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-23,288,487 , GRCh38.p12 chr15: 22,584,609-23,102,647 LOC729900, RN7SL495P, 15 more genes
    nsv6634460copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-23,282,799 , GRCh38.p12 chr15: 22,590,297-23,102,647 PDCD6IPP1, LOC100133165, 14 more genes
    nsv6634429copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,739,497-28,566,579 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 20,534,259-28,321,433 OR11J7P, SNORD115-21, 364 more genes
    nsv6623041copy number variation1nstd224human GRCh37 chr15: 22,574,927-23,769,205 , GRCh38.p12 chr15: 22,286,976-23,524,058 ABCB10P1, GOLGA6L2, 44 more genes
    nsv6622819copy number variation12nstd224human GRCh37 chr15: 20,603,222-20,871,548 , GRCh38.p12 chr15: 20,397,969-20,666,219 , GRCh38.p12 chr15|NT_187604.1: 1-140,294 GOLGA8EP, LOC401805, 15 more genes
    nsv6505909copy number variation1nstd223human GRCh38 chr15: 22,508,401-23,226,900 , GRCh37.p13 chr15: 22,646,194-23,364,695 WHAMMP3, HERC2P2, 23 more genes
    nsv6503108copy number variation1nstd223human GRCh38 chr15: 22,572,301-22,573,000 , GRCh37.p13 chr15: 23,300,096-23,300,795 HERC2P2
    nsv6500978copy number variation1nstd223human GRCh38 chr15: 22,449,284-28,543,944 , GRCh37.p13 chr15: 23,564,855-28,789,090 , PWRN3, 195 more genes
    nsv6315523copy number variation1nstd102humanUncertain significance GRCh37 chr15: 22,770,421-23,283,811 , GRCh38.p12 chr15: 22,589,285-23,102,647 PDCD6IPP1, LOC100133165, 14 more genes
    nsv6315468copy number variation1nstd102humanUncertain significance GRCh37 chr15: 23,011,467-23,620,154 , GRCh38.p12 chr15: 22,358,243-22,861,601 GOLGA8EP, LOC101927846, 20 more genes
    nsv6309608copy number variation2nstd102humanUncertain significance GRCh37 chr15: 23,006,221-23,932,364 , GRCh38.p12 chr15: 22,358,243-22,866,847 GOLGA8IP, GOLGA6L22, 21 more genes
    nsv6307588copy number variation1nstd186human GRCh37 chr15: 23,296,475-23,302,854 , GRCh38.p12 chr15: 22,570,242-22,576,621 , GRCh38.p12 chr15|NT_187604.1: 214,455-220,852 HERC2P2
    nsv6306475copy number variation1nstd186human GRCh37 chr15: 23,338,854-23,344,996 , GRCh38.p12 chr15|NT_187604.1: 172,318-178,460 , GRCh38.p12 chr15: 22,528,100-22,534,242 HERC2P2
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