arhgap35[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4457444	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 47,313,394-47,446,351 , GRCh38.p12 chr19: 46,810,137-46,943,094	ARHGAP35, AP2S1, 2 more genes
nsv3910109	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 46,458,122-47,683,579 , GRCh37 chr19: 46,961,379-48,186,836 , NCBI36 chr19: 51,653,219-52,878,648	ARHGAP35, FKRP, 38 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ARHGAP35, 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	ARHGAP35, 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	ARHGAP35, LENG8, 2408 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	ARHGAP35, ZNF461, 735 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	ARHGAP35, MIR4324, 485 more genes
nsv3924836	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402	ARHGAP35, IGFL1P1, 145 more genes
nsv3918983	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 46,658,791-49,050,450 , GRCh37 chr19: 47,162,048-49,553,707 , NCBI36 chr19: 51,853,888-54,245,519	ARHGAP35, LOC105372432, 121 more genes
nsv4350827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279	ARHGAP35, LINC01595, 59 more genes
nsv3900160	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 46,404,248-48,488,721 , GRCh38.p12 chr19: 45,900,990-47,985,464	ARHGAP35, C5AR1, 84 more genes
nsv7137151	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 47,028,919-48,185,409 , GRCh38.p12 chr19: 46,525,662-47,682,152	ARHGAP35, C5AR1, 36 more genes
nsv3907578	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 47,450,549-47,880,338 , GRCh38.p12 chr19: 46,947,292-47,377,081	ARHGAP35, C5AR1, 11 more genes
nsv4676350	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920	ARHGAP35, NKPD1, 112 more genes
nsv4676254	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 47,331,662-48,234,260 , GRCh38.p12 chr19: 46,828,405-47,731,003	ARHGAP35, AP2S1, 22 more genes
nsv3900603	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 46,918,881-47,782,258 , GRCh38.p12 chr19: 46,415,624-47,279,001	ARHGAP35, SAE1, 27 more genes
nsv3909504	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 47,228,251-47,867,279 , GRCh38.p12 chr19: 46,724,994-47,364,022	ARHGAP35, CCDC9, 17 more genes

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