dbVar for Gene (Select 134701) - 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
nsv7098884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093	LOC105377879, LOC100421583, 47 more genes
nsv7097461	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,563,136-84,567,108 , GRCh38.p12 chr6: 83,853,417-83,857,389	RIPPLY2
nsv7097460	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,563,136-84,563,512 , GRCh38.p12 chr6: 83,853,417-83,853,793	RIPPLY2
nsv6816854	copy number variation	1	nstd229	human		GRCh38 chr6: 83,298,441-83,971,760 , GRCh37.p13 chr6: 84,008,160-84,681,479	RIPPLY2, ME1, 4 more genes
nsv6808509	copy number variation	1	nstd229	human		GRCh38 chr6: 83,813,054-84,141,075 , GRCh37.p13 chr6: 84,522,773-84,850,794	MRAP2, RIPPLY2, 3 more genes
nsv6799076	copy number variation	1	nstd229	human		GRCh38 chr6: 83,830,159-83,909,852 , GRCh37.p13 chr6: 84,539,878-84,619,571	RIPPLY2, CYB5R4
nsv6791212	copy number variation	1	nstd229	human		GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389	SH3BGRL2, LCAL1, 93 more genes
nsv6636520	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,373,743-85,044,270 , GRCh38.p12 chr6: 83,664,024-84,334,552	CYB5R4, CEP162, 5 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	MTHFD2P2, RPL7P27, 212 more genes
nsv6631464	copy number variation	1	nstd224	human		GRCh37 chr6: 84,567,037-84,635,498 , GRCh38.p12 chr6: 83,857,318-83,925,779	RIPPLY2, CYB5R4
nsv6631270	copy number variation	1	nstd224	human		GRCh37 chr6: 84,563,879-84,594,649 , GRCh38.p12 chr6: 83,854,160-83,884,930	CYB5R4, RIPPLY2
nsv6563283	inversion	1	nstd223	human		GRCh38 chr6: 83,497,722-83,901,118 , GRCh37.p13 chr6: 84,207,441-84,610,837	SNAP91, CYB5R4, 3 more genes
nsv6412551	copy number variation	1	nstd223	human		GRCh38 chr6: 83,645,506-84,340,870 , GRCh37.p13 chr6: 84,355,225-85,050,588	CEP162, CYB5R4, 5 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	LOC101928570, RNU4-72P, 288 more genes
nsv6290989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748	KRT18P30, LOC107986620, 58 more genes
nsv5970982	inversion	1	nstd209	human		GRCh38 chr6: 83,497,669-83,901,098 , GRCh37.p13 chr6: 84,207,388-84,610,817	SNAP91, CYB5R4, 3 more genes
nsv5381391	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 83,878,953-84,567,108 , GRCh38.p12 chr6: 83,169,234-83,857,389	DOP1A, LOC105377879, 6 more genes
nsv5313423	copy number variation	1	nstd204	human		GRCh37.p13 chr6: 84,427,007-84,573,758 , GRCh38.p13 chr6: 83,717,288-83,864,039	CYB5R4, RIPPLY2, 1 more genes
nsv5230092	copy number variation	1	nstd204	human		GRCh38.p13 chr6: 83,856,283-83,857,482 , GRCh37.p13 chr6: 84,566,002-84,567,201	RIPPLY2
nsv5169729	mobile element insertion	1	nstd203	human		GRCh38 chr6: 83,853,120-83,853,136 , GRCh37.p13 chr6: 84,562,839-84,562,855	RIPPLY2

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Number of Variants: 20

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