dbVar for Gene (Select 105370035) - 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
nsv7148098	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 121,890,923-122,473,333 , GRCh38.p12 chr12: 121,453,120-122,035,427	BCL7A, HPD, 14 more genes
nsv7148095	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887	ANAPC5, MLXIP, 82 more genes
nsv7137030	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 122,281,739-122,292,608 , GRCh38.p12 chr12: 121,843,833-121,854,702	HPD, TIALD
nsv7136987	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 122,295,339-122,296,592 , GRCh38.p12 chr12: 121,857,433-121,858,686	HPD, TIALD
nsv7094203	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032	SBNO1, MIR9902-1, 58 more genes
nsv6934866	copy number variation	1	nstd229	human		GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647	RNU6-1088P, LOC105370042, 130 more genes
nsv6929031	copy number variation	1	nstd229	human		GRCh38 chr12: 121,862,093-121,866,821 , GRCh37.p13 chr12: 122,299,999-122,304,727	TIALD, HPD
nsv6927041	copy number variation	1	nstd229	human		GRCh38 chr12: 121,868,801-121,875,040 , GRCh37.p13 chr12: 122,306,707-122,312,946	TIALD, HPD
nsv6920920	copy number variation	1	nstd229	human		GRCh38 chr12: 121,001,001-122,266,400 , GRCh37.p13 chr12: 121,438,804-122,750,947	BCL7A, KDM2B, 36 more genes
nsv6919035	copy number variation	1	nstd229	human		GRCh38 chr12: 121,853,711-121,867,079 , GRCh37.p13 chr12: 122,291,617-122,304,985	HPD, TIALD
nsv6587020	inversion	1	nstd223	human		GRCh38 chr12: 121,868,769-121,869,333 , GRCh37.p13 chr12: 122,306,675-122,307,239	HPD, TIALD
nsv6583876	inversion	1	nstd223	human		GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521	RPL11P5, RPL17P37, 159 more genes
nsv6577806	inversion	1	nstd223	human		GRCh38 chr12: 121,874,437-121,874,936 , GRCh37.p13 chr12: 122,312,343-122,312,842	HPD, TIALD
nsv6576693	inversion	1	nstd223	human		GRCh38 chr12: 121,865,033-121,865,560 , GRCh37.p13 chr12: 122,302,939-122,303,466	HPD, TIALD
nsv6290266	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 121,887,337-123,386,068 , GRCh38.p12 chr12: 121,449,534-122,901,521	LINC02985, DENR, 38 more genes
nsv6290239	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809	ACADS, BCL7A, 356 more genes
nsv6132413	copy number variation	1	nstd213	human		GRCh37 chr12: 121,590,000-123,620,001 , GRCh38.p12 chr12: 121,152,197-123,135,454	BCL7A, HPD, 51 more genes
nsv6132140	copy number variation	1	nstd213	human		GRCh37 chr12: 122,300,000-122,420,001 , GRCh38.p12 chr12: 121,862,094-121,982,095	HPD, PSMD9, 3 more genes
nsv6038801	copy number variation	1	nstd212	human		GRCh38 chr12: 121,869,112-121,869,189 , GRCh37.p13 chr12: 122,307,018-122,307,095	TIALD, HPD
nsv6022613	copy number variation	1	nstd212	human		GRCh38 chr12: 121,874,489-121,874,584 , GRCh37.p13 chr12: 122,312,395-122,312,490	TIALD, HPD

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 212

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Number of Variants: 20

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