clns1a[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	CLNS1A, FAUP4, 2031 more genes
nsv3921121	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688	CLNS1A, LOC105369441, 296 more genes
nsv3915804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895	CLNS1A, TPBGL, 173 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	CLNS1A, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	CLNS1A, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	CLNS1A, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	CLNS1A, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	CLNS1A, SESN3, 694 more genes
nsv4456403	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 77,276,494-77,430,704 , GRCh38.p12 chr11: 77,565,449-77,719,659	CLNS1A, RSF1, 4 more genes
nsv6637911	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 77,211,136-78,014,355 , GRCh38.p12 chr11: 77,500,091-78,303,309	CLNS1A, RPS20P27, 22 more genes
nsv3909688	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 76,895,239-77,568,340 , GRCh38.p12 chr11: 77,184,194-77,857,294	CLNS1A, AQP11, 11 more genes

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