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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5672814copy number variation1nstd102humanPathogenic GRCh37 chr14: 50,778,709-50,778,888 , GRCh38.p12 chr14: 50,311,991-50,312,170 DMAC2L, L2HGDH
    nsv4999322copy number variation1nstd200human GRCh38 chr14: 50,314,929-50,323,304 , GRCh37.p13 chr14: 50,781,647-50,790,022 DMAC2L
    nsv4841892copy number variation1nstd200human GRCh37 chr14: 50,777,597-50,777,674 , GRCh38.p12 chr14: 50,310,879-50,310,956 L2HGDH, DMAC2L
    nsv4831603copy number variation1nstd200human GRCh37 chr14: 50,781,647-50,790,022 , GRCh38.p12 chr14: 50,314,929-50,323,304 DMAC2L
    nsv4679632copy number variation1nstd189human GRCh37.p13 chr14: 50,421,903-50,824,723 , GRCh38.p12 chr14: 49,955,185-50,358,005 SOS2, CDKL1, 12 more genes
    nsv4675996copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,317,272-51,627,752 , GRCh38.p12 chr14: 49,850,554-51,161,034 TRIM9, LINC01588, 32 more genes
    nsv4632655copy number variation1nstd183human GRCh37 chr14: 50,198,095-51,541,608 , GRCh38.p12 chr14: 49,731,377-51,074,890 , ABHD12B, 37 more genes
    nsv4632499copy number variation1nstd183human GRCh37 chr14: 50,394,890-50,905,488 , GRCh38.p12 chr14: 49,928,172-50,438,770 L2HGDH, LINC01599, 13 more genes
    nsv4629838copy number variation1nstd183human GRCh37 chr14: 49,986,935-50,930,979 , GRCh38.p12 chr14: 49,520,217-50,464,261 , RNU6-189P, 37 more genes
    nsv4623203copy number variation1nstd183human GRCh37 chr14: 49,893,688-50,942,527 , GRCh38.p12 chr14: 49,426,970-50,475,809 , LOC105378179, 38 more genes
    nsv4456447copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,737,668-50,799,764 , GRCh38.p12 chr14: 50,270,950-50,333,046 MIR4504, DMAC2L, 2 more genes
    nsv4339595sequence alteration1nstd166human GRCh37.p13 chr14: 50,526,988-51,369,623 , GRCh38.p12 chr14: 50,060,270-50,902,905 , DMAC2L, 17 more genes
    nsv4218878copy number variation1nstd166human GRCh37.p13 chr14: 50,724,321-53,837,159 , GRCh38.p12 chr14: 50,257,603-53,370,441 , SAV1, 60 more genes
    nsv3920804copy number variation1nstd102humanLikely benign NCBI36 chr14: 49,681,633-49,862,318 , GRCh38 chr14: 50,145,165-50,325,850 , GRCh37 chr14: 50,611,883-50,792,568 L2HGDH, MIR4504, 3 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
    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
    nsv3911849copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 38,735,127-56,250,932 , GRCh37 chr14: 39,665,376-57,181,179 , GRCh38 chr14: 39,196,172-56,714,461 ARF6, BMP4, 219 more genes
    nsv3911178copy number variation1nstd102humanUncertain significance NCBI36 chr14: 49,627,618-51,313,793 , GRCh37 chr14: 50,557,868-52,244,043 , GRCh38 chr14: 50,091,150-51,777,325 TRIM9, LINC01599, 35 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
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