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Items: 18

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    Number of Variants: 18

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908814copy number variation1nstd102humanBenign GRCh37 chr14: 62,487,438-62,509,647 , GRCh38.p12 chr14: 62,020,720-62,042,929 SYT16
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 SYT16, PARP1P2, 160 more genes
    nsv3923965copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803 SYT16, ESR2, 111 more genes
    nsv3924033copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999 SYT16, DACT1, 105 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 SYT16, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 SYT16, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 SYT16, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 SYT16, DHRS7, 1946 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 SYT16, SRMP2, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 SYT16, CRIP1, 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 SYT16, MIR656, 1918 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 SYT16, PAPOLA-DT, 1338 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 SYT16, PARP1P2, 91 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 SYT16, ACTN1, 400 more genes
    nsv4729599copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 61,409,856-65,742,610 , GRCh38.p12 chr14: 60,943,138-65,275,892 SYT16, PARP1P2, 73 more genes
    nsv4455801copy number variation1nstd102humanUncertain significance GRCh37 chr14: 61,126,208-63,517,651 , GRCh38.p12 chr14: 60,659,490-63,050,933 SYT16, LOC105370529, 26 more genes
    nsv4685707copy number variation1nstd102humannot provided GRCh37 chr14: 61,701,451-62,960,957 , GRCh38.p12 chr14: 61,234,733-62,494,239 SYT16, LINC00644, 16 more genes
    nsv4450515copy number variation1nstd102humannot provided GRCh37 chr14: 61,701,451-62,960,957 , GRCh38.p12 chr14: 61,234,733-62,494,239 SYT16, LOC105370525, 16 more genes
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