dbVar for Gene (Select 107075114) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6867601	copy number variation	1	nstd229	human		GRCh38 chr9: 74,649,401-74,866,500 , GRCh37.p13 chr9: 77,264,317-77,481,416	RN7SKP47, RNY4P1, 4 more genes
nsv6634454	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944	HNRNPA1P41, GAS1RR, 1868 more genes
nsv6315405	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032	RNU6-156P, GDA, 1425 more genes
nsv6313900	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132	ABCA1, ALAD, 793 more genes
nsv6313827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484	RPSAP75, ANKRD20A2P, 1008 more genes
nsv6313546	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937	FAM27C, DPM2, 2166 more genes
nsv6313110	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh38.p12 chr9: 74,497,977-74,887,856 , GRCh37 chr9: 77,112,893-77,502,772	RNY4P1, RORB, 6 more genes
nsv6290004	inversion	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378	ACO1, PLIN2, 1215 more genes
nsv6137094	copy number variation	1	nstd213	human		GRCh37 chr9: 71,840,000-78,800,001 , GRCh38.p12 chr9: 69,225,084-76,185,085	KLF9, PCSK5, 83 more genes
nsv4954839	copy number variation	1	nstd200	human		GRCh38 chr9: 74,637,212-74,987,883 , GRCh37.p13 chr9: 77,252,128-77,602,799	RN7SKP47, C9orf40, 9 more genes
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877	RPL35AP21, LOC105376097, 134 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4436161	complex substitution	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888	ACO1, ALDH1A1, 779 more genes
nsv4370451	copy number variation	1	nstd173	human		GRCh37 chr9: 77,245,240-77,602,921 , GRCh38.p12 chr9: 74,630,324-74,988,005	RN7SKP47, CARNMT1, 9 more genes
nsv3923526	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 74,029,084-79,136,863 , GRCh37 chr9: 74,839,264-79,947,043 , GRCh38 chr9: 72,224,348-77,332,127	GCNT1, NMRK1, 65 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3921710	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr9: 74,282,586-75,968,293 , GRCh37 chr9: 76,897,502-78,583,209 , NCBI36 chr9: 76,087,322-77,773,029	RNU6-1228P, NMRK1, 20 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PGAP4, ECPAS, 2167 more genes
nsv3920777	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,259,583-78,057,599 , GRCh38 chr9: 68,454,847-76,252,863 , GRCh37 chr9: 71,130,848-78,867,779	ANXA1, LOC105376080, 96 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 109

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Number of Variants: 20

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