sycn[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
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	SYCN, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	SYCN, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	SYCN, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	SYCN, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	SYCN, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	SYCN, ZNF461, 735 more genes
nsv3912447	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688	SYCN, MIR8077, 233 more genes
nsv3895066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003	SYCN, RNU6-140P, 162 more genes
nsv7095205	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932	SYCN, CCNP, 81 more genes
nsv7095479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147	SYCN, HNRNPL, 45 more genes
nsv3912394	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 44,054,509-44,534,649 , GRCh37.p13 chr19: 39,362,669-39,842,809 , GRCh38.p12 chr19: 38,872,029-39,352,169	SYCN, SAMD4B, 20 more genes

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sycn[All Fields] AND 1[has_clinical] (12)
dbVar
Rattus norvegicus ATP-binding cassette, sub-family D (ALD), member 4 (Abcd4), mR...
Rattus norvegicus ATP-binding cassette, sub-family D (ALD), member 4 (Abcd4), mRNA
gi|117414144|ref|NM_001013100.2|

Nucleotide
C0684328 (0)
MedGen
KIF20A kinesin family member 20A [Homo sapiens]
KIF20A kinesin family member 20A [Homo sapiens]
Gene ID:10112

Gene
Gene Links for GEO Profiles (Select 30489340) (1)
Gene

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