dbVar for Gene (Select 5047) - 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
nsv5920002	copy number variation	1	nstd209	human		GRCh38 chr9: 135,563,240-135,563,335 , GRCh37.p13 chr9: 138,455,086-138,455,181	PAEP
nsv4973315	copy number variation	1	nstd200	human		GRCh38 chr9: 135,559,237-135,564,374 , GRCh37.p13 chr9: 138,451,083-138,456,220	PAEP, LOC107987040
nsv4843100	copy number variation	1	nstd200	human		GRCh37 chr9: 138,451,083-138,456,220 , GRCh38.p12 chr9: 135,559,237-135,564,374	LOC107987040, PAEP
nsv4728050	copy number variation	2	nstd197	human		GRCh38.p12 chr9: 135,549,309-135,562,433 , GRCh37 chr9: 138,441,155-138,454,279	PAEP, OBP2A, 1 more genes
nsv4685995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549	TPRN, CCDC183, 137 more genes
nsv4684240	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 137,880,493-138,781,516 , GRCh38.p12 chr9: 134,988,647-135,889,670	LINC01502, LOC107987040, 25 more genes
nsv4675108	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 138,023,579-138,498,904 , GRCh38.p12 chr9: 135,131,733-135,607,058	PAEPP1, LINC02907, 15 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
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
nsv4454125	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 138,455,646-138,458,646 , GRCh38 chr9: 135,563,800-135,566,800	PAEP
nsv4453311	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 134,379,574-138,678,377 , GRCh38.p12 chr9: 131,504,187-135,786,531	RNU6ATAC, RPL21P81, 114 more genes
nsv3966657	copy number variation	1	nstd168	human		GRCh38 chr9: 135,561,612-135,605,251 , GRCh37.p13 chr9: 138,453,458-138,497,097	LOC105376316, PAEP, 2 more genes
nsv3924922	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 133,504,071-138,159,073 , NCBI36 chr9: 135,314,179-140,173,346 , GRCh37 chr9: 136,324,358-141,053,525	SETP5, NRARP, 178 more genes
nsv3923661	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 138,056,830-139,331,499 , NCBI36 chr9: 137,196,651-138,451,320 , GRCh38 chr9: 135,164,984-136,437,047	CAMSAP1, NACC2, 41 more genes
nsv3922926	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 137,483,683-139,628,011 , GRCh37 chr9: 138,343,862-140,508,190 , GRCh38 chr9: 135,452,016-137,613,738	SSNA1, LOC107987140, 126 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
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
nsv3920829	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497	LOC101928786, NRON, 495 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	ABHD17B, LOC100533707, 2167 more genes
nsv3920355	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 135,773,014-140,173,346 , GRCh38 chr9: 133,918,071-138,159,073 , GRCh37 chr9: 136,783,193-141,053,525	SLC34A3, OBP2A, 172 more genes

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Has Clinical Interpretation

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Number of Variants: 20

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