washc1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 13,997-11,376,705 , GRCh38.p12 chr9: 13,997-11,376,705	WASHC1, DMAC1, 136 more genes
nsv3912384	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,993-9,894,905 , GRCh37.p13 chr9: 12,993-9,904,905 , GRCh38.p12 chr9: 12,993-9,904,905	WASHC1, LOC105375951, 131 more genes
nsv3916544	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-2,780,382 , GRCh37.p13 chr9: 12,934-2,790,382 , GRCh38.p12 chr9: 12,934-2,790,382	WASHC1, H3P29, 44 more genes
nsv4684191	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 1-190,938 , GRCh37.p13 chr9: 10,001-190,938	WASHC1, PGM5P3, 10 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	WASHC1, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	WASHC1, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	WASHC1, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	WASHC1, OR13C1P, 2183 more genes
nsv3915734	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 13,997-71,015,981 , NCBI36 chr9: 3,997-70,205,801 , GRCh38 chr9: 13,997-68,401,065	WASHC1, CHCHD4P3, 866 more genes
nsv3907430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 13,997-70,919,878 , GRCh38.p12 chr9: 13,997-68,304,962	WASHC1, LOC105379448, 861 more genes
nsv3921759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-65,222,364 , GRCh37.p13 chr9: 12,934-65,482,544 , GRCh38.p12 chr9: 12,934-66,233,120	WASHC1, SPATA31A6, 824 more genes
nsv3919798	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-19,767,918 , GRCh37.p13 chr9: 12,934-19,777,918 , GRCh38.p12 chr9: 12,934-19,777,920	WASHC1, PLPP6, 222 more genes
nsv3871956	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr9: 10,000-400,952 , GRCh37.p13 chr9: 10,001-400,952	WASHC1, FOXD4, 13 more genes
nsv6634409	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729	WASHC1, ACO1, 594 more genes
nsv3902459	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 13,997-118,241 , GRCh38.p12 chr9: 13,997-118,241	WASHC1, MIR1302-9, 7 more genes
nsv3890274	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 10,590-364,675 , GRCh38.p12 chr9: 10,590-364,675	WASHC1, DDX11L5, 13 more genes
nsv3905478	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 21,234-191,843 , GRCh38.p12 chr9: 21,234-191,843	WASHC1, MIR1302-9HG, 9 more genes
nsv3920901	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr9: 2,934-281,236 , GRCh37.p13 chr9: 12,934-291,236 , GRCh38.p12 chr9: 12,934-291,236	WASHC1, MIR1302-9, 12 more genes

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