gsg1l2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6637454	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 9,695,852-10,118,691 , GRCh38.p12 chr17: 9,792,535-10,215,374	GSG1L2, NPM1P45, 3 more genes
nsv4681489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 9,698,245-10,451,247 , GRCh38.p12 chr17: 9,794,928-10,547,930	GSG1L2, MYH2, 11 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	GSG1L2, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	GSG1L2, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	GSG1L2, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	GSG1L2, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	GSG1L2, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	GSG1L2, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	GSG1L2, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	GSG1L2, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	GSG1L2, SLC2A4, 401 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	GSG1L2, C17orf49, 209 more genes
nsv1398516	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 9,701,182-11,983,353 , GRCh37 chr17: 9,604,499-11,886,670	GSG1L2, SCO1, 29 more genes
nsv3899694	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,431,013-9,868,179 , GRCh38.p12 chr17: 7,527,696-9,964,862	GSG1L2, VAMP2, 109 more genes
nsv3902311	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,929,776-9,995,862 , GRCh38.p12 chr17: 8,026,458-10,092,545	GSG1L2, RCVRN, 74 more genes
nsv4436354	complex substitution	1	nstd102	human	Uncertain significance	GRCh37 chr17: 9,586,165-16,325,968 , GRCh38.p12 chr17: 9,682,848-16,422,654	GSG1L2, ADORA2B, 109 more genes

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