zcchc9[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4456925	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 80,501,001-80,600,333 , GRCh38.p12 chr5: 81,205,182-81,304,514	ZCCHC9, CKMT2, 2 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	ZCCHC9, MEGF10, 2080 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	ZCCHC9, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	ZCCHC9, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	ZCCHC9, SPEF2, 2490 more genes
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	ZCCHC9, CSNK1A1P3, 413 more genes
nsv4675667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166	ZCCHC9, LOC101929380, 318 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	ZCCHC9, RNU1-150P, 1757 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	ZCCHC9, LOC105378993, 2492 more genes
nsv3879552	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 79,625,636-80,884,586 , GRCh38.p12 chr5: 80,329,817-81,588,767	ZCCHC9, CKMT2, 21 more genes
nsv3883879	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 79,678,575-80,868,550 , GRCh38.p12 chr5: 80,382,756-81,572,731	ZCCHC9, RASGRF2-AS1, 17 more genes
nsv4456362	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 79,664,621-80,767,791 , GRCh38.p12 chr5: 80,368,802-81,471,972	ZCCHC9, CKMT2, 17 more genes

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