cnksr3[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
nsv3911475	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407	CNKSR3, SNORA116, 275 more genes
nsv3913213	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240	CNKSR3, LDHAL6FP, 258 more genes
nsv6313530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314	CNKSR3, RSPH3, 144 more genes
nsv3916405	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984	CNKSR3, LOC112267968, 126 more genes
nsv7148221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958	CNKSR3, RNU6-824P, 97 more genes
nsv3903110	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 153,647,248-158,255,989 , GRCh38.p12 chr6: 153,326,113-157,834,957	CNKSR3, MTCO2P31, 49 more genes
nsv6291028	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 153,584,880-157,203,309 , GRCh38.p12 chr6: 153,263,745-156,882,175	CNKSR3, NMTRV-TAC1-1, 40 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	CNKSR3, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	CNKSR3, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	CNKSR3, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	CNKSR3, ITPR3, 2905 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	CNKSR3, LOC105369171, 418 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	CNKSR3, KATNA1, 422 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	CNKSR3, UST-AS2, 394 more genes
nsv3908622	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 150,284,435-170,919,470 , GRCh38.p12 chr6: 149,963,299-170,610,382	CNKSR3, LOC105378120, 319 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	CNKSR3, HYMAI, 263 more genes
nsv3904213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 151,214,792-170,892,243 , GRCh38.p12 chr6: 150,893,656-170,583,155	CNKSR3, CTAGE13P, 304 more genes
nsv3913037	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,697,473-170,921,089 , GRCh38 chr6: 152,376,338-170,612,001 , NCBI36 chr6: 152,739,166-170,763,014	CNKSR3, KRT8P44, 283 more genes
nsv4456488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222	CNKSR3, PDCL3P5, 176 more genes
nsv4436131	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067	CNKSR3, ACAT2, 303 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 27

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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