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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5593681copy number variation1nstd207human GRCh38 chr14: 92,719,159-92,719,386 , GRCh37.p13 chr14: 93,185,504-93,185,731 LGMN
    nsv5512332copy number variation1nstd206human GRCh38 chr14: 92,703,561-92,703,624 , GRCh37.p13 chr14: 93,169,906-93,169,969 LGMN
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5496394copy number variation1nstd206human GRCh38 chr14: 92,691,929-92,778,966 , GRCh37.p13 chr14: 93,158,274-93,245,311 LGMN
    nsv4849508copy number variation1nstd200human GRCh37 chr14: 93,207,516-93,208,111 , GRCh38.p12 chr14: 92,741,171-92,741,766 LGMN
    nsv4740865copy number variation1nstd199human GRCh37 chr14: 93,185,479-93,185,572 , GRCh38.p12 chr14: 92,719,134-92,719,227 LGMN
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4530625copy number variation1nstd166human GRCh37.p13 chr14: 93,185,545-93,185,689 , GRCh38.p12 chr14: 92,719,200-92,719,344 LGMN
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4230684copy number variation1nstd166human GRCh37.p13 chr14: 93,168,342-93,172,758 , GRCh38.p12 chr14: 92,701,997-92,706,413 LGMN
    nsv4224462copy number variation1nstd166human GRCh37.p13 chr14: 93,208,114-93,208,971 , GRCh38.p12 chr14: 92,741,769-92,742,626 LGMN
    nsv4214923copy number variation1nstd166human GRCh37.p13 chr14: 93,213,000-93,219,000 , GRCh38.p12 chr14: 92,746,655-92,752,655 LGMN
    nsv3922566copy number variation1nstd102humanPathogenic GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786 RPSAP4, LOC105370622, 97 more genes
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 more genes
    nsv3921292copy number variation1nstd102humanPathogenic GRCh38 chr14: 91,455,861-106,832,642 , GRCh37 chr14: 91,922,205-107,240,869 , NCBI36 chr14: 90,991,958-106,311,914 IGHVII-15-1, LINC03117, 594 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3918128copy number variation1nstd102humanUncertain significance GRCh38 chr14: 92,694,709-92,905,919 , NCBI36 chr14: 92,230,807-92,629,860 , GRCh37 chr14: 93,161,054-93,560,107 GOLGA5, LINC02287, 2 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3915681copy number variation1nstd102humanPathogenic NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298 IGHV3-32, SNORD114-31, 751 more genes
    nsv3914983copy number variation1nstd102humanPathogenic GRCh38 chr14: 86,094,030-106,832,642 , GRCh37 chr14: 86,560,374-107,240,869 , NCBI36 chr14: 85,630,127-106,311,914 IGHD5-5, EML5, 658 more genes
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