dbVar for Gene (Select 100133163) - 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
nsv7148270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-20,508,931 , GRCh38.p12 chr22: 18,483,514-20,345,217	DGCR2, MIR4761, 79 more genes
nsv7148246	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,838-21,416,074 , GRCh38.p12 chr22: 18,339,130-21,061,785	ZDHHC8, FAM230E, 121 more genes
nsv7148214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,609,932-21,576,553 , GRCh38.p12 chr22: 18,339,630-21,222,264	IGLL4P, LOC107985584, 129 more genes
nsv7137150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,888-21,481,925 , GRCh38.p12 chr22: 18,339,130-21,127,636	LOC107985584, LINC00896, 125 more genes
nsv7098862	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 18,206,749-21,234,326 , GRCh37.p13 chr22: 18,689,516-21,588,615	GP1BB, IGLL4P, 132 more genes
nsv7098756	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,886-21,386,103 , GRCh38.p12 chr22: 18,339,130-21,031,814	CCDC188, MED15, 118 more genes
nsv7095928	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 17,565,982-20,052,185 , GRCh38.p12 chr22: 17,085,092-20,064,662	CA15P1, BID, 103 more genes
nsv7093409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,893,888-21,570,386 , GRCh38.p12 chr22: 18,339,130-21,216,097	FAM247A, P2RX6P, 129 more genes
nsv7093403	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,184,000-21,416,024 , GRCh38.p12 chr22: 18,339,130-21,061,735	LOC105372862, RPL7AP70, 121 more genes
nsv7093402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,894,078-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528	LOC100420103, P2RX6P, 121 more genes
nsv7093382	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,834,445-21,414,817 , GRCh38.p12 chr22: 18,339,130-21,060,528	DGCR8, SEPTIN5, 121 more genes
nsv6638022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,843-21,075,592 , GRCh38.p12 chr22: 18,339,130-20,721,304	FAM230J, LOC107985588, 107 more genes
nsv6638009	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,648,867-21,465,659 , GRCh38.p12 chr22: 18,166,100-21,111,370	KLHL22, THAP7-AS1, 130 more genes
nsv6637960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,046,677-21,465,662 , GRCh38.p12 chr22: 18,339,130-21,111,373	TSSK2, LOC112268297, 125 more genes
nsv6637923	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-18,916,828 , GRCh38.p12 chr22: 16,408,174-18,929,315	ANKRD62P1, IGKV1OR22-1, 87 more genes
nsv6637871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 19,647,905-21,153,690 , GRCh38.p12 chr22: 18,339,130-20,799,402	GGTLC5P, C22orf39, 108 more genes
nsv6637775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,843-21,798,907 , GRCh38.p12 chr22: 18,339,130-21,444,618	CRKL, E2F6P3, 139 more genes
nsv6637764	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 18,560,247-18,916,828 , GRCh38.p12 chr22: 18,077,481-18,929,315	LOC101060852, FAM230J, 30 more genes
nsv6637709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,648,867-21,798,907 , GRCh38.p12 chr22: 18,166,100-21,444,618	FAM230A, GSC2, 144 more genes
nsv6637680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,916,828-21,800,797 , GRCh38.p12 chr22: 18,339,130-21,446,508	ABHD17AP4, E2F6P3, 139 more genes

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dbVar

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 897

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Number of Variants: 20

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