dhx29[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912667	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 54,572,751-54,653,868 , GRCh37 chr5: 54,536,994-54,618,111 , GRCh38 chr5: 55,241,166-55,322,283	DHX29, MTREX
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	DHX29, MEGF10, 2080 more genes
nsv3923429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770	DHX29, ISCA1P1, 163 more genes
nsv3922909	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 50,462,100-55,862,985 , GRCh37 chr5: 49,757,934-55,158,813 , NCBI36 chr5: 49,793,691-55,194,570	DHX29, HMGB1P47, 72 more genes
nsv7097148	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680	DHX29, RPL37P25, 69 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	DHX29, 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	DHX29, 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	DHX29, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	DHX29, LINC02241, 878 more genes
nsv3920391	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725	DHX29, KRT18P56, 290 more genes
nsv3878755	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 53,784,524-54,985,838 , GRCh38.p12 chr5: 54,488,694-55,690,010	DHX29, MIR449C, 26 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	DHX29, 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	DHX29, LOC105378993, 2492 more genes
nsv3913817	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 45,566,963-55,802,320 , GRCh38 chr5: 45,566,861-56,506,493 , NCBI36 chr5: 45,602,720-55,838,077	DHX29, LINC02118, 90 more genes
nsv4451131	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 53,180,658-54,552,379 , GRCh38.p12 chr5: 53,884,828-55,256,551	DHX29, HSPB3, 25 more genes
nsv3917640	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 54,359,842-55,271,282 , GRCh38 chr5: 55,028,257-55,939,697 , GRCh37 chr5: 54,324,085-55,235,525	DHX29, MIR449C, 24 more genes
nsv4456103	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 54,527,018-55,436,536 , GRCh38.p12 chr5: 55,231,190-56,140,709	DHX29, HNRNPH1P3, 20 more genes

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