kcp[All Fields] AND 1[has_clinical] - 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
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	KCP, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	KCP, LOC107986817, 2014 more genes
nsv3916726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440	KCP, LOC107986845, 245 more genes
nsv3903275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 127,295,698-139,524,358 , GRCh38.p12 chr7: 127,655,644-139,824,559	KCP, RNU6-1272P, 224 more genes
nsv6313876	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839	KCP, IMPDH1, 174 more genes
nsv3910648	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 124,170,657-134,163,594 , GRCh37 chr7: 123,810,711-133,848,346 , NCBI36 chr7: 123,597,947-133,498,886	KCP, CPA1, 165 more genes
nsv6313722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221	KCP, IRF5, 153 more genes
nsv4455826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163	KCP, ASB15, 127 more genes
nsv3923164	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016	KCP, GCC1, 104 more genes
nsv3915522	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 126,859,732-132,750,936 , NCBI36 chr7: 126,287,022-132,086,236 , GRCh37 chr7: 126,499,786-132,435,696	KCP, LRRC4, 126 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	KCP, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	KCP, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	KCP, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	KCP, TRGV3, 2682 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	KCP, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	KCP, CYP3A5, 1144 more genes
nsv4675620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017	KCP, RPL26P23, 887 more genes
nsv3918979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817	KCP, ABCF2, 844 more genes
nsv3917337	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 121,863,759-159,335,865 , NCBI36 chr7: 121,291,049-158,821,316 , GRCh37 chr7: 121,503,813-159,128,555	KCP, INSIG1-DT, 776 more genes
nsv4349183	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530	KCP, LOC105375582, 686 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 28

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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